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$NBIO ***Alert*** Nascent Biotech Inc. ***Alert***
2 Cancer Drugs
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
No convertibles
Moves on air
$NBIO Share Structure:
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
$NBIO ***Alert*** Nascent Biotech Inc. ***Alert***
2 Cancer Drugs
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
No convertibles
Moves on air
$NBIO Share Structure:
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
$DIS ripping here...This has been a head scratcher for me this entire bull market cycle. I still think it should be trading over $150. All WS wants to focus on is ESPN and cord cutting. Stock has been stuck in the mud.
ZERO
NFLX crushed...
$NBIO Nascent Biotech Inc.
Unpolished gem...wont be under the radar much longer.
2 Cancer Drugs
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
Clean Level 2
No convertibles
Moves on air
$NBIO Share Structure:
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
$NBIO Nascent Biotech Inc.
Unpolished gem...wont be under the radar much longer.
2 Cancer Drugs
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
Clean Level 2
No convertibles
Moves on air
$NBIO Share Structure:
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
$NBIO Share Structure: Clean L2, No Dilution, No Debt, No Convertible Note
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
NBIO closes at .55. Good day. So much more to come.
NBIO closes at .55. Good day. So much more to come.
$NBIO .55 X .58
Its getting tight the move is coming fellas, there are no shares available.
8,000,000 Float
$NBIO .55 X .58
Its getting tight the move is coming fellas, there are no shares available.
8,000,000 Float
$NBIO Nascent Biotech Inc.
Won't be under the radar much longer.
Current Price .565 Green 14.14%
2 Cancer Drugs
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
Clean Level 2
No convertibles
Moves on air
$NBIO Share Structure:
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
$NBIO Nascent Biotech Inc.
Won't be under the radar much longer.
Current Price .565 Green 14.14%
2 Cancer Drugs
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
Clean Level 2
No convertibles
Moves on air
$NBIO Share Structure:
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
$NBIO Nascent Biotech Inc. .565
***NBIO***NBIO***NBIO***
Won't be under the radar much longer.
2 Cancer Drugs
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
Clean Level 2
No convertibles
Moves on air
$NBIO Share Structure:
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
$NBIO Nascent Biotech Inc. .565
***NBIO***NBIO***NBIO***
Won't be under the radar much longer.
2 Cancer Drugs
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
Clean Level 2
No convertibles
Moves on air
$NBIO Share Structure:
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
$NBIO Nascent Biotech Inc.
***NBIO***NBIO***NBIO***
Won't be under the radar much longer.
2 Cancer Drugs
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
Clean Level 2
No convertibles
Moves on air
$NBIO Share Structure:
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
$NBIO Nascent Biotech Inc.
***NBIO***NBIO***NBIO***
Won't be under the radar much longer.
2 Cancer Drugs
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
Clean Level 2
No convertibles
Moves on air
$NBIO Share Structure:
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
$NBIO Nascent Biotech Inc.
Unpolished gem...wont be under the radar much longer.
2 Cancer Drugs
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
Clean Level 2
No convertibles
Moves on air
$NBIO Share Structure:
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
$NBIO Nascent Biotech Inc.
Unpolished gem...wont be under the radar much longer.
2 Cancer Drugs
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
Clean Level 2
No convertibles
Moves on air
$NBIO Share Structure:
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
$NBIO Nascent Biotech Inc. ***POUNDING THE TABLE HERE FELLAS***
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
Clean Level 2
No convertibles
Moves on air
$NBIO Share Structure:
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing
$NBIO Nascent Biotech Inc. ***POUNDING THE TABLE HERE FELLAS***
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
Clean Level 2
No convertibles
Moves on air
$NBIO Share Structure:
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
$NBIO ***Alert*** Nascent Biotech Inc. ***Alert***
2 Cancer Drugs
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
Clean Level 2
No convertibles
Moves on air
$NBIO Share Structure:
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
$NBIO...100% Absolute real undervalued company with FDA news on the way.
8,000,000 share float, tight and wound. Ten grand in dollar volume and this shoots over a dollar.
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
$NBIO Nascent Biotech Inc.
Unpolished gem...wont be under the radar much longer.
2 Cancer Drugs
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
Clean Level 2
No convertibles
Moves on air
$NBIO Share Structure:
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
$NBIO Nascent Biotech Inc.
Unpolished gem...wont be under the radar much longer.
2 Cancer Drugs
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
Clean Level 2
No convertibles
Moves on air
$NBIO Share Structure:
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
$NBIO tic toc tic toc
2 Cancer Drugs
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
Clean Level 2
No convertibles
Moves on air
$NBIO Share Structure:
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
$NBIO getting healthier. Bid ask getting tighter. No sellers at the bid. Time is ticking. Starting to get wound pretty tight.
2 Cancer Drugs
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
Clean Level 2
No convertibles
Moves on air
$NBIO Share Structure:
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
$NBIO getting healthier. Bid ask getting tighter. No sellers at the bid. Time is ticking. Starting to get wound pretty tight.
2 Cancer Drugs
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
Clean Level 2
No convertibles
Moves on air
$NBIO Share Structure:
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
CDEL is literally the only thing holding $NBIO down. When they are cleared out this will fly. Some people just don't understand how to trade or build wealth.
$NBIO ***Alert*** Nascent Biotech Inc. ***Alert***
2 Cancer Drugs
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
Clean Level 2
No convertibles
Moves on air
$NBIO Share Structure:
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
StockGoodies...This is the play of the year!!!
NBIO ***Alert***
2 Cancer Drugs
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
Clean Level 2
No convertibles
Moves on air
$NBIO Share Structure:
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
Volume coming in today!!!! The big push over a dollar is coming. Smart money loading up.
NBIO ***Alert
2 Cancer Drugs
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
Clean Level 2
No convertibles
Moves on air
NBIO ***Alert*** $NBIO ***Pounding The Table** $NBIO
2 Cancer Drugs
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
Clean Level 2
No convertibles
Moves on air
$5.00 by end of the year buy out target.
High Alert!!!
NBIO ***Alert*** $NBIO ***Pounding The Table** $NBIO
2 Cancer Drugs
Human trials coming
No debt
No dilution
OTCQB Fully Reporting
Transparent TA
8,000,000 Float
Clean Level 2
No convertibles
Moves on air
$5.00 by end of the year buy out target.
High Alert!!!
$NBIO Completly Under the Radar: Chck it out!!!!
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
$NBIO Completly Under the Radar: Chck it out!!!!
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
$NBIO Share Structure: Clean L2, No Dilution, No Debt, No Convertible Note
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.
$NBIO Share Structure: Clean L2, No Dilution, No Debt, No Convertible Note
Outstanding Shares
28,543,295
07/03/2018
Restricted
20,133,185
07/03/2018
Float
8,410,110
07/03/2018
Nascent Biotech Significant Milestones Achieved since 2015
Re-engineered antibody into CHO cells: The original cell line was created as a Hybridoma. Manufacturing from the Hybridoma cell line was a prohibitively expensive very process. A recombinant form was created that secretes over 40 fold more antibodies.
Created and fully characterized and qualified Master Cell Bank (MCB):
Produced 400+ grams of GMP grade mAb: This is a key inflection point with Biotech Investors which mitigates manufacturing risk. Formulation studies show that the antibodies are stable.
Pre-IND and clinical protocol discussions with FDA: There were no preclinical issues and the FDA provided guidance for our Study Protocol which increases the probability that we will gain IND approval on the first attempt. This also mitigates IND trial delays.
Settled $1.7M debt to license holder
Retired debenture – eliminating 30% shareholder dilution.
Finished in life phase toxicology studies (monkey and rat): “This is the easiest study I have ever seen. I wish all my Toxicology Studies went this well,” Fred Reno-Toxicology trial consultant. Completing the toxicology study mitigates toxicology issues. Nascent had none.
Completed Viral Clearance study – Significantly exceeds FDA recommendations.
Completed Fill and Finish of purified bulk product.
Filed IND Application April 2017 – Finalizing FDA requested studies. Plan to refile by mid Q 1 2018 (FDA requested a new Viral Clearance Study and a Tox/Clinical lot Comparative Analysis).
Signed $16 Million licensing deal with Hisun Pharmaceuticals for Mainland China - $ 3 million received in upfront payment – Saved investors significant dilution.
Raised $1.45 Million in equity investment – no debt financing.