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I noticed the volume.... I like it.
I am a low volume, high tech-biotech bottom feeder LOL
Love to hear more, to hear the rest of the story. I have an investor group that follows my DD, mostly focused Biotechs and related plays these days.
Tell me more please.
Locked float ecomike. 55% is insider held. Another 35% is like family and friebds of insiders. Been in this play for 3 years. This isnt your ordinary corona pump play you see quite a bit these days. Company is still relatively unknown. This thing moves on 30k shares traded lol. Wait until we get some real volume this thing will pop.
Wow, this thing $ACHFF either has no float or one hell of a locked up float looking at the volume.
I like! I do not many know about it yet.
The year of the Pandemic, Drug-Biotech life line rally, will extend into next year.
Daily rate of new cases world wide hit an all time record 2 days ago, 330,000 new cases in one day.
124 Million annual rate and rising exponentially.
I will adding ACHFF to my Biotech drug retirement stock list.
Dosing should start soon (possibly this week). If it shows any signs of working this things going to take off.
ARch Biopartners Inc (ACHFF)
1.0 ? -0.01 (-0.99%)
Volume: 4,224 @09/24/20 1:58:04 PM EDT
Bid Ask Day's Range
0.95 1.02 1.0 - 1.0
ACHFF Detailed Quote
ARch Biopartners Inc (ACHFF)
1.015 ? -0.015 (-1.46%)
Volume: 2,395 @09/04/20 12:19:14 PM EDT
Bid Ask Day's Range
0.96 1.02 1.007168 - 1.015
ACHFF Detailed Quote
ARch Biopartners Inc (ACHFF)
1.03 ? 0.0235 (2.33%)
Volume: 10,303 @08/14/20 3:07:34 PM EDT
Bid Ask Day's Range
0.98 1.04 1.03 - 1.0335
ACHFF Detailed Quote
ARch Biopartners Inc (ACHFF)
1.03 ? 0.0235 (2.33%)
Volume: 10,303 @08/14/20 3:07:34 PM EDT
Bid Ask Day's Range
0.98 1.04 1.03 - 1.0335
ACHFF Detailed Quote
$ACHFF ARch Biopartners Inc (ACHFF)
0.9366 ? 0.0 (0.00%)
Volume: 0 @-
Bid Ask Day's Range
0.5904 3.06 - - -
ACHFF Detailed Quote
$ACHFF , I AGREE
RE;
Sleeper company with amazing potential. Good share structure,
good management, and a potentially amazing product.
This is one of those lottery ticket type stocks.
Could be a home run.
Treating kidney and lung inflammation.
These types of stocks are very far and in between.
At $1.52 a share this thing is an absolute steal
$ACHFF Arch Biopartners submits IND to the FDA for COVID-19 Phase II trial to prevent organ inflammation.
June 08 2020 - 08:30AM
InvestorsHub NewsWire Print
TORONTO, Canada -- June 8, 2020 -- InvestorsHub NewsWire -- Arch Biopartners Inc. (“Arch” or the “Company”) (TSX Venture: ARCH and OTCQB: ACHFF), a clinical stage company developing new drug candidates for treating organ damage caused by inflammation,
today announced it has submitted an Investigational New Drug (IND) Application to the U.S. Food and Drug Administration (FDA) for its lead drug Metablok (LSALT peptide) to conduct a Phase II trial to prevent acute organ inflammation and injury experienced by patients with COVID-19.
The submission of the IND application was made by Arch following several weeks of review of the Company’s Phase II plans by the FDA under the Coronavirus Treatment Acceleration Program.
The Phase II trial, which was recently cleared by Health Canada to proceed, will be a multicenter, randomized, double-blind, placebo-controlled, proof of concept study of LSALT peptide in COVID-19. The trial is expected to commence in the summer of 2020.
The primary endpoint of the Phase II trial is a composite that includes prevention of acute respiratory distress syndrome (ARDS), acute kidney injury (AKI), and acute liver injury.
The composite reflects severe effects often experienced by hospitalized COVID-19 patients and Metablok’s novel mechanism of action in blocking consequential inflammation in these organs.
About COVID-19
COVID-19 is the disease caused by the novel coronavirus SARS-CoV-2 that emerged in China in late 2019. Patients with severe COVID-19 develop progressive lung inflammation and acute respiratory distress syndrome that often requires mechanical ventilation and critical care.
Patients with severe COVID-19 also experience multiple organ dysfunction including acute kidney injury, liver dysfunction, cardiac failure, and blood abnormalities. Currently, no approved vaccine or effective antiviral drug exists for SARS-CoV-2. Treatment of severe COVID-19 has been primarily supportive, relying on respiratory, infectious diseases, and critical care medicine.
Survival rates and health care system capacity could both be improved with new treatments that prevent the severe manifestations of COVID-19, such as worsening lung inflammation (ARDS) and AKI experienced by patients infected with SARS-CoV-2.
About Arch Biopartners
Arch Biopartners Inc. is a clinical stage company focused on the development of innovative technologies that have the potential to make a significant medical or commercial impact. Arch is developing a drug pipeline to produce new drug candidates that inhibit inflammation in the lungs, liver and kidneys caused via the dipeptidase-1 (DPEP-1) pathway.
Metablok (LSALT peptide) is a novel peptide drug candidate and the lead DPEP-1 inhibitor in the Arch development pipeline. In August 2019, a scientific team led by Arch scientists Dr. Donna Senger and Dr. Stephen Robbins published a paper in the journal Cell describing a novel mechanism of action for organ inflammation. In the publication, DPEP-1 was identified for the first time as a major neutrophil (white blood cell) adhesion receptor on the lung, liver and kidney endothelium.
A total of 40 out of 52 healthy, normal volunteers received Metablok during the recent placebo-controlled Phase I human trial.
In all cases, Metablok was well tolerated during the trial and no significant drug-related adverse effects were observed.
Continuing under development in the Arch portfolio are: AB569, a potential new treatment for antibiotic resistant bacterial infections in the lung and wounds; and, ‘Borg’ peptide coatings that increase corrosion resistance and decrease bacterial biofilm on various medical grade metals and plastics.
For more information on Arch Biopartners, its technologies and other public documents Arch has filed on SEDAR, please visit www.archbiopartners.com
The Company has 59,882,302 common shares outstanding.
Forward-Looking Statements
All statements, other than statements of historical fact, in this news release are forward looking statements that involve various risks and uncertainties, including, without limitation, statements regarding the future plans and objectives of the Company. There can be no assurance that such statements will prove to be accurate. Actual results and future events could differ materially from those anticipated in such statements. These and all subsequent written and oral forward-looking statements are based on the estimates and opinions of management on the dates they are made and are expressly qualified in their entirety by this notice. The Company assumes no obligation to update forward-looking statements should circumstances or management’s estimates or opinions change.
Neither TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release
For more information, please contact:
Richard Muruve
Chief Executive Officer
Arch Biopartners, Inc.
647-428-7031
e. info@archbiopartners.com
ARch Biopartners Inc (ACHFF)
0.99718 ? 0.0 (0.00%)
Volume: 0 @-
Bid Ask Day's Range
0.6561 1.07 - - -
ACHFF Detailed Quote
$achff Arch Biopartners submits IND to the FDA for COVID-19 Phase II trial to prevent organ inflammation.
June 08 2020 - 08:30AM
InvestorsHub NewsWire Print
TORONTO, Canada -- June 8, 2020 -- InvestorsHub NewsWire -- Arch Biopartners Inc. (“Arch” or the “Company”) (TSX Venture: ARCH and OTCQB: ACHFF), a clinical stage company developing new drug candidates for treating organ damage caused by inflammation, today announced it has submitted an Investigational New Drug (IND) Application to the U.S. Food and Drug Administration (FDA) for its lead drug Metablok (LSALT peptide) to conduct a Phase II trial to prevent acute organ inflammation and injury experienced by patients with COVID-19.
The submission of the IND application was made by Arch following several weeks of review of the Company’s Phase II plans by the FDA under the Coronavirus Treatment Acceleration Program.
The Phase II trial, which was recently cleared by Health Canada to proceed, will be a multicenter, randomized, double-blind, placebo-controlled, proof of concept study of LSALT peptide in COVID-19. The trial is expected to commence in the summer of 2020.
The primary endpoint of the Phase II trial is a composite that includes prevention of acute respiratory distress syndrome (ARDS), acute kidney injury (AKI), and acute liver injury. The composite reflects severe effects often experienced by hospitalized COVID-19 patients and Metablok’s novel mechanism of action in blocking consequential inflammation in these organs.
About COVID-19
COVID-19 is the disease caused by the novel coronavirus SARS-CoV-2 that emerged in China in late 2019. Patients with severe COVID-19 develop progressive lung inflammation and acute respiratory distress syndrome that often requires mechanical ventilation and critical care. Patients with severe COVID-19 also experience multiple organ dysfunction including acute kidney injury, liver dysfunction, cardiac failure, and blood abnormalities. Currently, no approved vaccine or effective antiviral drug exists for SARS-CoV-2. Treatment of severe COVID-19 has been primarily supportive, relying on respiratory, infectious diseases, and critical care medicine.
Survival rates and health care system capacity could both be improved with new treatments that prevent the severe manifestations of COVID-19, such as worsening lung inflammation (ARDS) and AKI experienced by patients infected with SARS-CoV-2.
About Arch Biopartners
Arch Biopartners Inc. is a clinical stage company focused on the development of innovative technologies that have the potential to make a significant medical or commercial impact. Arch is developing a drug pipeline to produce new drug candidates that inhibit inflammation in the lungs, liver and kidneys caused via the dipeptidase-1 (DPEP-1) pathway.
Metablok (LSALT peptide) is a novel peptide drug candidate and the lead DPEP-1 inhibitor in the Arch development pipeline. In August 2019, a scientific team led by Arch scientists Dr. Donna Senger and Dr. Stephen Robbins published a paper in the journal Cell describing a novel mechanism of action for organ inflammation. In the publication, DPEP-1 was identified for the first time as a major neutrophil (white blood cell) adhesion receptor on the lung, liver and kidney endothelium.
A total of 40 out of 52 healthy, normal volunteers received Metablok during the recent placebo-controlled Phase I human trial. In all cases, Metablok was well tolerated during the trial and no significant drug-related adverse effects were observed.
Continuing under development in the Arch portfolio are: AB569, a potential new treatment for antibiotic resistant bacterial infections in the lung and wounds; and, ‘Borg’ peptide coatings that increase corrosion resistance and decrease bacterial biofilm on various medical grade metals and plastics.
For more information on Arch Biopartners, its technologies and other public documents Arch has filed on SEDAR, please visit www.archbiopartners.com
The Company has 59,882,302 common shares outstanding.
Forward-Looking Statements
All statements, other than statements of historical fact, in this news release are forward looking statements that involve various risks and uncertainties, including, without limitation, statements regarding the future plans and objectives of the Company. There can be no assurance that such statements will prove to be accurate. Actual results and future events could differ materially from those anticipated in such statements. These and all subsequent written and oral forward-looking statements are based on the estimates and opinions of management on the dates they are made and are expressly qualified in their entirety by this notice. The Company assumes no obligation to update forward-looking statements should circumstances or management’s estimates or opinions change.
Neither TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release
For more information, please contact:
Richard Muruve
Chief Executive Officer
Arch Biopartners, Inc.
647-428-7031
e. info@archbiopartners.com
ARch Biopartners Inc (ACHFF)
1.12 ? 0.0 (0.00%)
Volume: 0 @-
Bid Ask Day's Range
0.729 1.52 - - -
ACHFF Detailed Quote
Sleeper company with amazing potential. Good share structure, good management, and a potentially amazing product. This is one of those lottery ticket type stocks. Could be a home run. Treating kidney and lung inflammation. These types of stocks are very far and in between. At $1.52 a share this thing is an absolute steal
Arch Biopartners submits IND to the FDA for COVID-19 Phase II trial to prevent organ inflammation. InvestorsHub NewsWire - 6/8/2020 8:30:00 AM
A
Arch Biopartners Receives Health Canada Approval for COVID-19 Phase II Human Trial InvestorsHub NewsWire - 5/8/2020 8:03:48 AM
Arch Biopartners Applies to Health Canada to Conduct COVID19 Phase II Human Trial to Prevent Lung and Kidney Inflammation InvestorsHub NewsWire - 4/24/2020 7:18:15 AM
ARch Biopartners Inc (ACHFF)
1.1168 ? 0.0768 (7.38%)
Volume: 1,270 @06/08/20 10:29:23 AM EDT
Bid Ask Day's Range
1.05 1.08 1.1152 - 1.12
ACHFF Detailed Quote
Arch Biopartners Receives Health Canada Approval to Conduct COVID-19 Phase II Human Trial
May 08, 2020 06:00 ET | Source: Arch Biopartners
TORONTO, May 08, 2020 (GLOBE NEWSWIRE) -- Arch Biopartners Inc., (“Arch” or the “Company”) (TSX Venture: $ARCH and OTCQB: $ACHFF ) a clinical stage company developing new drug candidates for treating organ damage caused by inflammation, today announced it has received a No Objection Letter from Health Canada to conduct a Phase II human trial for its lead drug LSALT peptide (Metablok) to prevent organ inflammation experienced by patients with COVID-19.
The Phase II trial will be a multicenter, randomized, double-blind, placebo-controlled, proof of concept study of LSALT peptide. The primary endpoint is to prevent the development of life threatening acute respiratory distress syndrome (ARDS) in patients early in the course of COVID-19.
A secondary endpoint of the Phase II trial is to prevent kidney inflammation and injury, which also contributes to mortality and occurs in up to 30% of patients with severe COVID-19.
The trial will begin with the enrolment of 60 hospitalized patients who will receive either LSALT peptide or drug-free saline daily for up to 14 days. There will be an option to expand the study to include a larger number of subjects.
As a result of clinical interest to support the Phase II trial in the United States, Arch continues to be in dialogue with the U.S. Food and Drug Administration to obtain permission to recruit patients at American clinical sites into the trial.
About COVID-19
COVID-19 is the disease caused by the novel coronavirus SARS-CoV-2 that emerged in China in late 2019. Patients with severe COVID-19 develop progressive lung inflammation and acute respiratory distress syndrome that often requires mechanical ventilation and critical care. Patients with severe COVID-19 also experience multi-organ dysfunction including acute kidney injury, liver dysfunction, cardiac failure and blood abnormalities. Currently, no vaccine or effective antiviral drug exists for SARS-CoV-2. Treatment of COVID-19 has been primarily supportive, relying on critical care physicians.
Survival rates and health care system capacity could both be improved with new treatments that prevent the severe manifestations of COVID-19, such as worsening lung inflammation (ARDS) and acute kidney injury experienced by patients infected with SARS-CoV-2.
About Arch Biopartners
Arch Biopartners Inc. is a clinical stage company focused on the development of innovative technologies that have the potential to make a significant medical or commercial impact. Arch is developing a drug library to produce new drug candidates that inhibit inflammation in the lungs, liver and kidneys caused via the dipeptidase-1 (DPEP-1) pathway.
Metablok is a novel peptide drug candidate and the lead DPEP-1 inhibitor in the Arch development pipeline. In August 2019, a scientific team led by Arch scientists Dr. Donna Senger and Dr. Stephen Robbins published a paper in the journal Cell describing a novel mechanism of action for organ inflammation. In the publication, DPEP-1 was identified for the first time as a major neutrophil (white blood cell) adhesion receptor on the lung, liver and kidney endothelium.
A total of 40 out of 52 healthy, normal volunteers received Metablok during the recent Phase I human trial. In all cases, Metablok was well tolerated during this placebo-controlled trial and no significant drug-related adverse effects were observed.
Continuing under development in the Arch portfolio are: AB569, a potential new treatment for antibiotic resistant bacterial infections in the lung and wounds; and, ‘Borg’ peptide coatings that increase corrosion resistance and decrease bacterial biofilm on various medical grade metals and plastics.
For more information on Arch Biopartners, its technologies and other public documents Arch has filed on SEDAR, please visit www.archbiopartners.com
The Company has 59,882,302 common shares outstanding.
Forward-Looking Statements
All statements, other than statements of historical fact, in this news release are forward looking statements that involve various risks and uncertainties, including, without limitation, statements regarding the future plans and objectives of the Company. There can be no assurance that such statements will prove to be accurate. Actual results and future events could differ materially from those anticipated in such statements. These and all subsequent written and oral forward-looking statements are based on the estimates and opinions of management on the dates they are made and are expressly qualified in their entirety by this notice. The Company assumes no obligation to update forward-looking statements should circumstances or management’s estimates or opinions change.
Neither TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release
For more information, please contact:
Richard Muruve
Chief Executive Officer
Arch Biopartners, Inc.
647-428-7031
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545 King Street West
P.O. Box 305
Toronto, ONT M5V 1M1
Canada
TORONTO, July 14, 2020 (GLOBE NEWSWIRE) -- Arch Biopartners Inc. (“Arch” or the “Company”) (TSX Venture: ARCH and OTCQB: ACHFF),
a clinical stage company developing new drug candidates for treating organ damage caused by inflammation, today announced it has engaged a leading,
global contract research organization to initiate and conduct a Phase II trial in the U.S. for its lead drug Metablok (LSALT peptide)
to treat complications in patients with COVID-19 including the prevention of acute lung and/or kidney injury.
The Phase II trial will be a multicenter, randomized, double-blind, placebo-controlled, proof of concept study of LSALT peptide as prevention of acute
respiratory distress syndrome (ARDS) and acute kidney injury (AKI) in sixty patients infected with SARS-CoV-2 (COVID-19).
Following guidance and discussion with the FDA during the review of the Phase II protocol, the primary endpoint of the trial was expanded to a composite that includes prevention of ARDS and AKI.
The composite reflects severe effects often experienced by hospitalized COVID-19 patients and deemed appropriate for LSALT peptide’s novel mechanism of action in blocking consequential inflammation in these organs.
“We have focused our efforts to conduct the Phase II trial in the U.S., where there has been a significant increase in COVID-19 infections.
We look forward to working with our new CRO and U.S. hospital sites as we try to increase survival rates of hospitalized COVID-19 patients
at risk of lung and kidney inflammation,” said Richard Muruve, CEO of Arch.
About COVID-19
COVID-19 is the disease caused by the novel coronavirus SARS-CoV-2 that emerged in China in late 2019. Severe complications from COVID-19
are in large part due to excessive host immune responses to the virus that result in progressive lung inflammation and
acute respiratory distress syndrome that often requires mechanical ventilation and critical care1.
Patients with severe COVID-19 also experience multiple organ dysfunction including acute kidney injury, liver dysfunction, cardiac failure, and blood abnormalities.
Currently, no approved vaccine or effective antiviral drug exists for SARS-CoV-2. Treatment of severe COVID-19 has been primarily supportive,
relying heavily on respiratory, infectious disease and critical care medicine.
Survival rates and health care system capacity could both be improved with new treatments that prevent the severe manifestations of COVID-19,
such as worsening lung inflammation (ARDS) and AKI experienced by patients infected with SARS-CoV-2.
1 J. S. Ayres, Sci. Adv 10.1126/sciadv.abc1518 (2020)
About Arch Biopartners
Arch Biopartners Inc. is a clinical stage company focused on the development of innovative technologies that have the potential to make a significant medical or commercial impact.
Arch is developing a drug pipeline to produce new drug candidates that inhibit inflammation in the lungs, liver and kidneys caused via the dipeptidase-1 (DPEP-1) pathway.
Metablok (LSALT peptide) is a novel peptide drug candidate and the lead DPEP-1 inhibitor in the Arch development pipeline.
In August 2019, a scientific team led by Arch scientists Dr. Donna Senger and Dr. Stephen Robbins published a paper in the journal Cell describing a novel mechanism of action for organ inflammation.
In the publication, DPEP-1 was identified for the first time as a major leukocyte (white blood cell) adhesion receptor on the lung, liver and kidney endothelium.
LSALT differs from typical anti-inflammatory drugs by targeting this novel adhesion receptor rather than targeting individual cytokines, of which there are over 30 currently known.
A total of 40 out of 52 healthy, normal volunteers received Metablok during the recent placebo-controlled Phase I human trial. In all cases,
Metablok was well tolerated during the trial and no significant drug-related adverse effects were observed.
Continuing under development in the Arch portfolio are: AB569, a potential new treatment for antibiotic resistant bacterial infections in the lung and wounds; and,
‘Borg’ peptide coatings that increase corrosion resistance and decrease bacterial biofilm on various medical grade metals and plastics.
For more information on Arch Biopartners, its technologies and other public documents Arch has filed on SEDAR, please visit
http://www.archbiopartners.com
The Company has 60,782,302 common shares outstanding.
Forward-Looking Statements
All statements, other than statements of historical fact, in this news release are forward looking statements that involve various risks and uncertainties,
including, without limitation, statements regarding the future plans and objectives of the Company.
There can be no assurance that such statements will prove to be accurate. Actual results and future events could differ materially from those anticipated in such statements.
These and all subsequent written and oral forward-looking statements are based on the estimates and opinions of management on the
dates they are made and are expressly qualified in their entirety by this notice.
The Company assumes no obligation to update forward-looking statements should circumstances or management’s estimates or opinions change.
The science and medical contents of this release have been approved by the Company’s Chief Science Officer
The Company is not making any express or implied claims that its product has the ability to eliminate, cure or contain Covid-19 (or SARS-2 Coronavirus) at this time
Neither TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release
For more information, please contact: Richard Muruve
Chief Executive Officer
Arch Biopartners, Inc.
647-428-7031
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