Register for free to join our community of investors and share your ideas. You will also get access to streaming quotes, interactive charts, trades, portfolio, live options flow and more tools.
Register for free to join our community of investors and share your ideas. You will also get access to streaming quotes, interactive charts, trades, portfolio, live options flow and more tools.
Agree, not everyone invests and holds for any length of time anymore. Most hold a day or two, capitalize on the quick pennies, others don't even hold overnight....then there are those that search, dd, buy, and sit tight and wait for the dollars instead of the pennies.
That's what we have here. Respect our own individual styles of investing/trading, etc.
Happy Friday!
Good morning BRICH and Yes sir!
I'm getting a kick out of all these new folks. I'm long and strong RLFTF, RVVTF, IPIX
Good morning everyone!
yes ma'am!!
absolutely...thank you for bringing this to light and reminding us all how fortunate we actually are. Pay it forward!!
3BB
You're welcome!
Hey bunky this is what I've found in dd.
Relief Therapeutics holds orphan drug designations from the U.S. Food and Drug Administration and the European Union for the use of VIP to treat ARDS, pulmonary hypertension, and sarcoidosis. Relief Therapeutics also holds a U.S. patent1 for RLF-100 and proprietary manufacturing processes for its synthesis.
What a fantastic day/weeks ahead!!
3BB
Excellent news! Thank you for being the first to post it. Fabulous advancements happening!
https://fintel.io/doc/sec-ipix-8k-innovation-pharmaceuticals-2020-august-04-18478
Security IPIX / Innovation Pharmaceuticals Inc (15115V101)
Form Type 8-K
File Date 2020-08-04
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
FORM 8-K
CURRENT REPORT PURSUANT TO
SECTION 13 OR 15(D) OF THE
SECURITIES EXCHANGE ACT OF 1934
Date of Report (Date of earliest event reported): July 31, 2020
INNOVATION PHARMACEUTICALS INC.
(Exact Name of Registrant as Specified in Charter)
Nevada
001-37357
30-0565645
(State or Other Jurisdiction
(Commission
(IRS Employer
of Incorporation)
File Number)
Identification No.)
301 Edgewater Place - Suite 100
Wakefield, Massachusetts
01880
(Address of Principal Executive Offices)
(Zip Code)
Registrant’s telephone number, including area code: (978) 921-4125
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):
? Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
? Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
? Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
? Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))
Securities registered under Section 12(b) of the Exchange Act: none
Indicate by check mark whether the Registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
Emerging growth company ?
If an emerging growth company, indicate by check mark if the Registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ?
Item 1.01 Entry into a Material Definitive Agreement.
On July 31, 2020, Innovation Pharmaceuticals Inc. (the “Company”) entered into a common stock purchase agreement (the “Purchase Agreement”) with Aspire Capital Fund, LLC (“Aspire Capital”) which provides that, upon the terms and subject to the conditions and limitations set forth therein, Aspire Capital is committed to purchase up to an aggregate of $30.0 million of shares of the Company’s Class A common stock (“common stock”) over the 24-month term of the Purchase Agreement. Concurrently with entering into the Purchase Agreement, the Company also entered into a registration rights agreement with Aspire Capital (the “Registration Rights Agreement”), in which the Company agreed to file with the Securities and Exchange Commission (the “SEC”) one or more registration statements, as necessary, and to the extent permissible and subject to certain exceptions, to register under the Securities Act of 1933, as amended, for the sale of the shares of the Company’s common stock that have been and may be issued to Aspire Capital under the Purchase Agreement. The Company has filed with the SEC a prospectus supplement to the Company’s effective shelf registration statement on Form S-3 (File No. 333-239817) registering all of the shares of common stock that may be offered to Aspire Capital from time to time.
Under the Purchase Agreement, on any trading day selected by the Company, the Company has the right, in its sole discretion, to present Aspire Capital with a purchase notice (each, a “Purchase Notice”), directing Aspire Capital (as principal) to purchase up to 1,000,000 shares of the Company’s common stock per business day, up to $30.0 million of the Company’s common stock in the aggregate, at a per share price (the “Purchase Price”) equal to the lesser of:
·
the lowest sale price of the Company’s common stock on the purchase date; or
·
the arithmetic average of the three (3) lowest closing sale prices for the Company’s common stock during the twelve (12) consecutive trading days ending on the trading day immediately preceding the purchase date.
The Company and Aspire Capital also may mutually agree to increase the number of shares that may be sold to as much as an additional 5,000,000 shares per business day.
In addition, on any date on which the Company submits a Purchase Notice to Aspire Capital in an amount equal to at least 1,000,000 shares, the Company also has the right, in its sole discretion, to present Aspire Capital with a volume-weighted average price purchase notice (each, a “VWAP Purchase Notice”) directing Aspire Capital to purchase an amount of stock equal to up to 30% of the aggregate shares of the Company’s common stock traded on its principal market on the next trading day (the “VWAP Purchase Date”), subject to a maximum number of shares the Company may determine. The purchase price per share pursuant to such VWAP Purchase Notice is generally 95% of the volume-weighted average price for the Company’s common stock traded on its principal market on the VWAP Purchase Date.
The Purchase Price will be adjusted for any reorganization, recapitalization, non-cash dividend, stock split, or other similar transaction occurring during the period(s) used to compute the Purchase Price. The Company may deliver multiple Purchase Notices and VWAP Purchase Notices to Aspire Capital from time to time during the term of the Purchase Agreement, so long as the most recent purchase has been completed.
2
The Purchase Agreement provides that the Company and Aspire Capital shall not effect any sales under the Purchase Agreement on any purchase date where the closing sale price of the Company’s common stock is less than $0.10. There are no trading volume requirements or restrictions under the Purchase Agreement, and the Company will control the timing and amount of sales of the Company’s common stock to Aspire Capital.Aspire Capital has no right to require any sales by the Company, but is obligated to make purchases from the Company as directed by the Company in accordance with the Purchase Agreement. There are no limitations on use of proceeds, financial or business covenants, restrictions on future fundings, rights of first refusal, participation rights, penalties or liquidated damages in the Purchase Agreement. In consideration for entering into the Purchase Agreement, on August 4, 2020 the Company issued to Aspire Capital 6,250,000 shares of the Company’s common stock (the “Commitment Shares”). The Purchase Agreement may be terminated by the Company at any time, at its discretion, without any cost to the Company. Aspire Capital has agreed that neither it nor any of its agents, representatives and affiliates shall engage in any direct or indirect short-selling or hedging of the Company’s common stock during any time prior to the termination of the Purchase Agreement. Any proceeds that the Company receives under the Purchase Agreement are expected to be used for working capital and general corporate purposes.
The foregoing is a summary description of certain terms of the Purchase Agreement and the Registration Rights Agreement and, by its nature, is incomplete. Copies of the Purchase Agreement and Registration Rights Agreement are filed herewith as Exhibits 10.1 and 4.1, respectively, to this Current Report on Form 8-K and are incorporated herein by reference. All readers are encouraged to read the entire text of the Purchase Agreement and the Registration Rights Agreement.
The legal opinion, including the related consent, of Gary R. Henrie relating to the issuance of shares of the Company’s common stock pursuant to the Purchase Agreement is filed as Exhibit 5.1 to this Current Report on Form 8-K.
Item 1.02 Termination of a Material Definitive Agreement.
Pursuant to the Purchase Agreement, the Company and Aspire Capital terminated the prior common stock purchase agreement, dated September 6, 2017, between the parties.
Item 7.01 Regulation FD Disclosure.
On August 4, 2020, the Company issued a press release titled, Innovation Pharmaceuticals and U.S. Regional Biocontainment Laboratory Nearing Completion of Brilacidin Anti-SARS-CoV-2 (COVID-19) In Vitro Testing.
A copy of the press release is furnished herewith as Exhibit 99.1. The information in this Current Report on Form 8-K under this Item 7.01, including the accompanying press release, shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended, nor shall it be deemed incorporated by reference in any filing under the Securities Act of 1933, as amended, except as shall be expressly set forth by reference to such filing.
Item 9.01 Financial Statements and Exhibits.
(d) Exhibits.
Exhibit No.
Description
4.1
Registration Rights Agreement, dated July 31, 2020, between Innovation Pharmaceuticals Inc. and Aspire Capital Fund, LLC
5.1
Opinion of Gary R. Henrie, Esq.
10.1
Common Stock Purchase Agreement, dated July 31, 2020, between Innovation Pharmaceuticals Inc. and Aspire Capital Fund, LLC
23.1
Consent of Gary R. Henrie, Esq. (included in Exhibit 5.1)
99.1
Press Release dated August 4, 2020
my pleasure and you're welcome! I'm glad many are finding the information useful.
NP...thought it was a worthwhile read.
Enron accountants know how to posture shady deals that's for sure. In Houston back in the day....what a scam
Nice aspect to point out. I read it but didn't realize the significance in terms of it being an important deviation from the original intent. Clearly indicates a higher degree of confidence by those assembling the testing criteria.
Thanks for pointing out and bringing to light such a significant element.
LOOKING UP Drug that gives fellas a lift in the bedroom may also beat Covid, experts believe
Shaun Wooller
5 Aug 2020, 23:03Updated: 5 Aug 2020, 23:03
A DRUG that gives fellas a lift in the bedroom may also beat Covid, experts believe.
Officials in the US have granted the £9.50 jab fast track approval after early signs of success.
?? Read our coronavirus live blog for the latest news & updates
A drug used to treat erectile dysfunction 'could beat Covid'
1
A drug used to treat erectile dysfunction 'could beat Covid'Credit: Getty - Contributor
It is still undergoing clinical trials but can already be used for emergency coronavirus cases.
Doctors at Houston Methodist Hospital say it helped one seriously ill man make a “rapid recovery”.
The patient, 54, developed Covid while being treated for rejection of a double lung transplant.
But he came off a ventilator within four days of treatment with RLF-100, or aviptadil.
More than 15 other critically ill patients are also said to have recovered from respiratory failure within three days of treatment.
The drug is used in the UK to treat erectile dysfunction. It is combined with phentolamine and injected into the privates.
Brazillian researchers found aviptadil stopped the coronovirus multiplying in human lung cells and immune cells in a lab.
MOST READ IN HEALTH NEWS
SKIN CRAWLINGItching, burning and tenderness are sign of 'new coronavirus symptom'
IN FOR THE LONG HAULBrits suffering 'long covid' as doctors 'dismiss long-term symptoms'
HOT SPOTSInteractive map reveals if coronavirus cases are rising in YOUR area
GULP!Paracetamol 'does more harm than good for chronic pain & shouldn't be prescribed'
CORONA RATINGWhat is the current R rate in my area? How to track it every day
KNOW THE SIGNSWhat is a persistent dry cough and is it a symptom of coronavirus?
Jonathan Javitt, from drug developer NeuroRx, said: “No other antiviral agent has demonstrated rapid recovery from viral infection and demonstrated laboratory inhibition of viral replication.” Medics are now awaiting the result of formal trials involving five US hospitals and 70 patients who are less sick.
Some have been given the real drug and others a placebo to see if there is a difference in outcomes.
It is hoped the drug will prevent the disease progressing when given at an earlier stage.
nice post and good montra to respect.
Thought I'd re-post a bit better aligned...apologies
Date High Low Close* Adj Close Volume
Aug 05, .2660 0.3500 0.2500 0.3060 0.3060 17,389,655
Aug 04, .2700 0.2835 0.2221 0.2500 0.2500 12,053,319
Aug 03, .3300 0.3940 0.2589 0.2900 0.2900 30,056,480
Jul 31, .1900 0.2950 0.1900 0.2945 0.2945 41,020,579
Jul 30, .1768 0.1939 0.1600 0.1775 0.1775 5,687,739
Jul 29, .2010 0.2010 0.1820 0.1856 0.1856 2,413,424
Important Post I read from a fellow IHUB'er. Valuable insight so I thought I'd share....
https://whenindoubtgetout.wordpress.com/2011/05/30/double-and-triple-prints/amp/?__twitter_impression=true&fbclid=IwAR38dcdicrsYazjM528iDFGcbVm8NXVrITbORyGh4aenlDs9kxNfzkZCEX4
Important Post I read from a fellow IHUB'er. Valuable insight so I thought I'd share....
https://whenindoubtgetout.wordpress.com/2011/05/30/double-and-triple-prints/amp/?__twitter_impression=true&fbclid=IwAR38dcdicrsYazjM528iDFGcbVm8NXVrITbORyGh4aenlDs9kxNfzkZCEX4
Are you in the stock yet. Been watching it for a few days. Looking at taking a starter position. Am I seeing right OS 1.8B? What's the float. Interesting tid-bit - back in 2019 when stock took huge hit and fell, gap down right at .11k, exactly where our gap up is today.
Anyhow, just looking for some solid insight, no p/d...want to take a solid "in" position. Feel like the company has some stamina and staying power.
GLTY
3BB
Date Open High Low Close* Adj Close** Volume
Aug 05, 2020 0.2660 0.3500 0.2500 0.3060 0.3060 17,389,655
Aug 04, 2020 0.2700 0.2835 0.2221 0.2500 0.2500 12,053,319
Aug 03, 2020 0.3300 0.3940 0.2589 0.2900 0.2900 30,056,480
Jul 31, 2020 0.1900 0.2950 0.1900 0.2945 0.2945 41,020,579
Jul 30, 2020 0.1768 0.1939 0.1600 0.1775 0.1775 5,687,739
Jul 29, 2020 0.2010 0.2010 0.1820 0.1856 0.1856 2,413,424
Love it!
Agree with you Mike, this stock always seems to sell off a tad at the very very end of the day. I wonder if it has anything to do with the trading trends on the other exchanges? Probably not
Welcome Curt!
Thanks and Best of luck to you too!
Yes...you're absolutely right.
Because I've been watching it for the past hour or two and seen it go from .28 to .21???
In the past few days (since last Friday) this stock is up over 400% if you just take it to .20.
A swing from .28 to .21 is a small fraction of pullback/retracement and consolidation and yes penny flippers flipping.
OTC and penny stocks are by nature volatile. .28 to .21 whether one entered a position at the low end when we traded last week or at current levels...IMHO patience should be easy to hold with what we have here!
GLTY and the very best of trading!!
3BB
Both RLFTF and RVVTF are SOLID investments
Brilacidin is showing consistent and robust antiviral activity across the viral lifecycle in human lung and Vero cells; potential as a treatment for preventing infection with COVID-19, as well as for treatment of patients once infected
Article to be submitted for peer-review publication in September, with pre-print made available
WAKEFIELD, Mass., Aug. 04, 2020 (GLOBE NEWSWIRE) -- Innovation Pharmaceuticals (OTCQB:IPIX)
Welcome Doug!
Beautiful movement upwards this morning. Foolish to sell at current levels..unless pennies and small margins are you're preference.
"to each his own"!
GLT----all RLFTF Investors!
You're welcome...any time!
Nice morning movement. Look forward to next 60 days. We keep referring to CYDY...it's major upward moves happend early January, March/April and June. Being long in a stock/investment/trade such as RVVTF is more than just looking at dailies. Perspective, DD, and knowing what you hold is paramount. Best to all you daily traders moving for pennies; my portfolio looks out beyond the daily horizon.
Best of LUCK to us all!
It appears on Yahoo Finance stats of stock symbol.
https://finance.yahoo.com/quote/RVVTF/key-statistics?p=RVVTF
AUG 5, 2020 Article piece
Houston Methodist reports rapid recovery of critically ill COVID-19 patients with new drug
Houston Methodist Hospital is making national headlines after doctors used a new drug to help treat critically ill COVID-19 patients.
Methodist was the first to report the rapid recovery of patients on ventilators and those with severe medical conditions after three days of treatment. The drug is called RLF-100 and is also known as aviptadil. It has been approved by the FDA for emergency use at multiple clinical sites in patients who are too ill to enter the FDA’s Phase 2/3 trials.
RLFTF
OS now lists at 163.9M. Happened yesterday
Same with ETRADE...$6.95
News just released.
Revive Therapeutics Update Following U.S. FDA Approval of Phase 3 Clinical Trial for Bucillamine in COVID-19
TORONTO, Aug. 05, 2020 (GLOBE NEWSWIRE) --
Revive Therapeutics Ltd. (“Revive” or the “Company”) (CSE: RVV, USA: RVVTF), a specialty life sciences company focused on the research and development of therapeutics for medical needs and rare disorders, is pleased to announce that following the U.S. Food & Drug Administration (“U.S. FDA”) approval to proceed with the Company’s Phase 3 clinical trial to evaluate the safety and efficacy of Bucillamine in patients with mild-moderate COVID-19, the Company is finalizing agreements and aligning resources to initiate the Phase 3 clinical trial in September.
“With the FDA approval of the Phase 3 clinical study to evaluate Bucillamine in the treatment of patients with mild-moderate COVID-19, our team and partners are working diligently to align our resources and expertise that will fast-track the Phase 3 study,” said Michael Frank, Revive’s Chief Executive Officer.
Revive expects to engage up to 10 clinical trial sites in the U.S. and open the Phase 3 clinical trial for patient screening in Q3-2020. The Company is finalizing vendor agreements in the project management, medical monitoring, data management and clinical packaging for the trials. In addition, Revive and its clinical trial partners will be evaluating potential U.S. clinical sites and clinical investigators in major COVID-19 affected U.S. states, such as Florida, California, Arizona and Texas.
About the Phase 3 Confirmatory Clinical Study
The Phase 3 confirmatory clinical study titled, “A Multi-Center, Randomized, Double-Blind, Placebo-Controlled Study of Bucillamine in Patients with Mild-Moderate COVID-19”, will enroll up to 1,000 patients that will be randomized 1:1:1 to receive Bucillamine 100 mg three times a day (“TID”), Bucillamine 200 mg TID or placebo TID for up to 14 days. The primary objective is to compare frequency of hospitalization or death in patients with mild-moderate COVID-19 receiving Bucillamine therapy with those receiving placebo. The primary endpoint is the proportion of patients meeting a composite endpoint of hospitalization or death from the time of first dose through Day 28 following randomization. Efficacy will be assessed by comparison of clinical outcome (death or hospitalization), disease severity using the 8-category NIAID COVID ordinal scale, supplemental oxygen use, and progression of COVID-19 between patients receiving standard-of-care plus Bucillamine (high dose and/or low dose) and patients receiving standard-of-care plus placebo. Safety will be assessed by reported pre-treatment adverse events and treatment-emergent adverse events (including serious adverse events and adverse events of special interest), laboratory values (hematology and serum chemistry), vital signs (heart rate, respiratory rate, and temperature), and peripheral oxygen saturation.
An interim analysis will be performed by an Independent Data and Safety Monitoring Board (“DSMB”) after 210 patients have been treated and followed up for a total of 28 days after randomization. The better performing Bucillamine dose at the interim analysis will be selected and patients will then be randomized 2:1 to the selected Bucillamine dose or placebo. Additional interim analyses will be performed after 400, 600, and 800 patients have reached this same post-treatment timepoint. The independent DSMB will actively monitor interim data for the ongoing safety of patients and will recommend continuation, stopping or changes to the conduct of the study based on the interim analysis reports.
The Company is not making any express or implied claims that its product has the ability to eliminate or cure COVID-19 (SARS-2 Coronavirus) at this time.
Scientific Rationale of Bucillamine for COVID-19
Preclinical and clinical studies have demonstrated that reactive oxygen species contribute to the destruction and programmed cell death of pulmonary epithelial cells.1 N-acetyl-cysteine (NAC) has been shown to significantly attenuate clinical symptoms in respiratory viral infections in animals and humans, primarily via donation of thiols to increase antioxidant activity of cellular glutathione2,3,4,5. Bucillamine (N-(mercapto-2-methylpropionyl)-l-cysteine) has a well-known safety profile and is prescribed in the treatment of rheumatoid arthritis in Japan and South Korea for over 30 years. Bucillamine, a cysteine derivative with two thiol groups, has been shown to be 16 times more potent as a thiol donor in vivo than NAC 6. The drug is non-toxic with high cellular permeability. The basis of the clinical study will analyze if Bucillamine has the potential, via increasing glutathione activity and other anti-inflammatory activity, to lessen the destructive consequences of SARS-CoV2 infection in the lungs and attenuate the clinical course of COVID-19.
About Revive Therapeutics Ltd.
Revive is a life sciences company focused on the research and development of therapeutics for infectious diseases and rare disorders, and it is prioritizing drug development efforts to take advantage of several regulatory incentives awarded by the FDA such as Orphan Drug, Fast Track, Breakthrough Therapy and Rare Pediatric Disease designations. Currently, the Company is exploring the use of Bucillamine for the potential treatment of infectious diseases, with an initial focus on severe influenza and COVID-19. With its recent acquisition of Psilocin Pharma Corp., Revive is advancing the development of Psilocybin-based therapeutics in various diseases and disorders. Revive’s cannabinoid pharmaceutical portfolio focuses on rare inflammatory diseases and the Company was granted FDA orphan drug status designation for the use of Cannabidiol (CBD) to treat autoimmune hepatitis (liver disease) and to treat ischemia and reperfusion injury from organ transplantation. For more information, visit www.ReviveThera.com.
For more information, please contact:
Michael Frank
Chief Executive Officer
Revive Therapeutics Ltd.
Tel: 1-888-901-0036
Email: mfrank@revivethera.com
Website: www.revivethera.com
This has a very strong chance of happening....it makes sense to expand usage of Aviptadil.
tendies - Thank you so much for all of the News Releases you spent your time seeking out and posting for the rest of us. Your dd is very much appreciated. Thanks again and GO RLFTF!!
Subscribe to Ad free and enjoy an ad-free experience
Try Now
Keep the Ads