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Thursday, May 13, 2021

CytoDyn in Distribution Pact with Macleods Pharma for EUA, Compassionate Use in India

 CytoDyn Inc. (OTC.QB: CYDY), (“CytoDyn” or the “Company"), a late-stage biotechnology company developing leronlimab (Vyrologix or PRO 140), a CCR5 antagonist with the potential for multiple therapeutic indications, announced today it has executed an exclusive supply and distribution agreement with Macleods Pharmaceuticals Ltd. in India. This commercial agreement will enable Macleods to sell leronlimab in India following regulatory clearance.

Nader Pourhassan, Ph.D., President and Chief Executive Officer of CytoDyn, stated, “We are delighted Macleods Pharmaceuticals reached out to CytoDyn and equally excited to reach this agreement with their team so quickly. From the time they first contacted us about our drug, we were able to conclude this agreement within a few days. It is an honor to work with an organization so motivated to bring leronlimab to COVID-19 patients in India. Currently India has zero product approved for critically ill Covid-19 patients and we are delighted to be working toward being the first approved drug for this population.”

Vijay Agarwal, a Business Development Director at Macleods, commented, “We are thrilled with our recently executed exclusive supply and distribution agreement with CytoDyn. We believe there is an immediate need for leronlimab in our country, to save COVID-19 infected patients who are on ventilators. We need to bring this product to market ASAP for them!”


Macleods, headquartered in Mumbai, India, is a vertically integrated, global pharmaceutical company. Established in 1986, Macleods features in top 10 pharmaceutical companies in India. Macleods specializes in the development and manufacturing of active pharmaceutical ingredients and finished dosage pharmaceutical formulations. More information is available at www.macleodspharma.com.

https://www.globenewswire.com/news-release/2021/05/13/2229152/19782/en/CytoDyn-Signs-Distribution-Agreement-with-Macleods-Pharmaceuticals-Ltd-to-Pursue-EUA-and-Compassionate-Use-Access-to-Leronlimab-in-India.html

Merck: Phase 3 Trial Met Primary Endpoints in High-Risk Early-Stage Triple-Negative Breast Cancer

 In Pivotal Study, KEYTRUDA® (pembrolizumab) In Combination With Chemotherapy Before Surgery and Continuing as a Single Agent After Surgery Showed Statistically Significant Improvement in EFS Versus Pre-Operative Chemotherapy

KEYTRUDA Is the First Anti-PD-1 Therapy to Show a Statistically Significant Improvement in EFS as Neoadjuvant and Adjuvant Therapy for TNBC

Merck (NYSE: MRK), known as MSD outside the United States and Canada, today announced positive results from the pivotal neoadjuvant/adjuvant Phase 3 KEYNOTE-522 trial investigating KEYTRUDA, Merck’s anti-PD-1 therapy, in combination with chemotherapy as pre-operative (neoadjuvant) treatment and then continuing as a single agent (adjuvant) treatment after surgery. KEYNOTE-522 met its dual primary endpoint of event-free survival (EFS) for the treatment of patients with high-risk early-stage triple-negative breast cancer (TNBC). Based on an interim analysis conducted by the independent Data Monitoring Committee (DMC), neoadjuvant KEYTRUDA plus chemotherapy followed by adjuvant KEYTRUDA as monotherapy showed a statistically significant and clinically meaningful improvement in EFS compared with neoadjuvant chemotherapy alone. As previously communicated, KEYNOTE-522 met its other dual primary endpoint of pathological complete response (pCR). The safety profile of KEYTRUDA in this trial was consistent with that observed in previously reported studies; no new safety signals were identified.

https://finance.yahoo.com/news/merck-announces-phase-3-keynote-104500585.html

Heron Gets FDA OK on Postoperative Pain Med

 ZYNRELEF is the first and only FDA-approved extended-release dual-acting local anesthetic, clinically proven to manage pain and to eliminate the need for opioids for up to 72 hours following surgery better than bupivacaine solution, the current standard-of-care -

- Full U.S. commercial launch of ZYNRELEF is planned for July 2021 -

- Conference call and webcast today at 8:30 am ET -

Conference Call and Webcast

Heron will host a conference call and webcast on May 13, 2021 at 8:30 am ET. The conference call can be accessed by dialing 877-311-5906 for domestic callers and 281-241-6150 for international callers. Please provide the operator with the passcode 3922347 to join the conference call. The conference call will also be available via webcast under the Investor Relations section of Heron's website at www.herontx.com. An archive of the teleconference and webcast will also be made available on Heron's website for 60 days following the call.

https://finance.yahoo.com/news/heron-therapeutics-announces-u-fda-120000741.html

Can Ocugen Overcome This Major Hurdle?

 Ocugen (NASDAQ:OCGN) is the biotech stock everyone's been talking about these past few months. The company made a splash when it said it was partnering with India's Bharat Biotech to bring an almost-ready coronavirus vaccine candidate to the U.S. market. As a result, Ocugen's shares have soared more than 400% so far this year.

The potential vaccine -- Covaxin -- is in phase 3 development in India. The country granted it emergency authorization earlier in the year. As part of the deal with Bharat, Ocugen stands to benefit from 45% of U.S. vaccine profits -- if the U.S. Food and Drug Administration (FDA) offers Covaxin authorization. But even if the FDA gives the product a nod, Ocugen still faces a major hurdle.

Ocugen's agreement with Bharat covers sales of Covaxin in the U.S. only. So, U.S. authorization represents Ocugen's only opportunity to generate revenue from Covaxin. Authorization isn't my biggest concern. Of course, the FDA may not be in a hurry to authorize newcomers since it already has authorized three coronavirus vaccines (those of ModernaPfizer and partner BioNTech, and Johnson & Johnson).

But eventually, it's in everyone's best interest to have a variety of products available. Each product has a characteristic that may make it the best choice for certain individuals. For instance, the J&J vaccine drew interest because it's the only vaccine administered in one dose. And considering the depth of the pandemic, it's preferable to have access to a broad range of vaccines.

So, if Covaxin's safety and efficacy meet the FDA's standards, we can imagine the agency offering the product authorization. This may take some time. It's not yet clear if the FDA will require Ocugen to conduct U.S.-based trials of Covaxin -- or if it will base a decision on data from the trials in India. In Ocugen's earnings report last week, the company said it has submitted data to the FDA and will add more as it comes in from Bharat. But a longer time to market isn't my concern.

The major hurdle facing Ocugen is demand. Or lack of it. President Joe Biden earlier this year bought enough vaccine doses from Pfizer and Moderna to cover most of the U.S. population. Now, Pfizer is about to roll out its vaccine to a new population: teens. The FDA authorized that earlier this week. Moderna is close behind. And both companies are testing their vaccines in children. We might even expect a vaccine rollout to that very youngest group later this year or in early 2022.


Biden recently spoke of donating extra vaccine supply to other countries that are struggling to obtain enough doses. So, it would be surprising if the U.S. actually ordered new vaccine doses in the near term.

Let's look further into the future. Once the U.S. has completed this first rollout and used up most doses, there will be a need for a whole new round of doses. Companies haven't confirmed the frequency of vaccination. But many experts say we should expect annual vaccines -- much like the flu.

That means Ocugen could vie for a share of the U.S. market farther down the road. But if the market leaders are able to bring the pandemic under control, it's likely these leaders will attract most of the future orders. This means there may not be much room left for Covaxin.

Of course, Ocugen doesn't have to be a market leader to benefit from Covaxin sales. Still, the Covaxin partnership represents an investment. Sales of the vaccine must cover the investment -- and generate enough to help Ocugen advance its main business. That main business is gene therapy for eye diseases.


And here, Ocugen has a long way to go. The company said in its earnings report that it is on target to begin four phase 1/2 trials by the end of next year. These represent the company's most advanced programs.

At this point, it's unclear whether a potential U.S. supply deal will compensate for Ocugen's investment in Covaxin. And considering the strength of today's market leaders, I'm not optimistic about Covaxin's potential to truly take off in the U.S.

So, in my view, Ocugen will struggle to overcome the hurdle of low demand in the U.S. All of that means a limited revenue opportunity. And if that indeed happens, it could be devastating for this high-flying stock in the long term.

https://www.fool.com/investing/2021/05/13/can-ocugen-overcome-this-major-hurdle/

CureVac: 2nd-Gen COVID Vax Shows High Immunogenicity vs. Variants

 CureVac N.V. (NASDAQ:CVAC), a global biopharmaceutical company developing a new class of transformative medicines based on messenger ribonucleic acid (mRNA), today announced together with its collaboration partner GSK, first preclinical data in a rat model, showing that its second-generation COVID-19 vaccine candidate, CV2CoV, induces high levels of antigen production as well as strong and dose-dependent immune responses in vaccinated animals. CV2CoV is a co-development between CureVac and GSK and is based on a new mRNA backbone, which differs from CureVac's first-generation vaccine candidate, CVnCoV, currently in late-stage clinical testing. Preclinical data in rats immunized with CV2CoV in the dose range of 0.5-40µg demonstrated fast onset of strong immune responses already after the first dose. In addition, the serum of vaccinated animals showed significant cross-neutralization against variants first discovered in Denmark (B.1.1.298), the UK (B.1.1.7) and South Africa (B.1.351). The full manuscript of the preclinical data is available on the pre-print server bioRxiv.

https://finance.yahoo.com/news/curevac-second-generation-covid-19-114500478.html

Celyad to Present Data on CAR T Candidate in Myeloma Trial at European Hematology Meet

 

  • No Grade ≥ 3 treatment-related adverse events nor evidence of Graft-versus-Host disease reported from the completed first dose-level (DL1) cohort of Phase 1 dose-escalation IMMUNICY-1 trial evaluating the shRNA-based anti-BCMA CAR T candidate, CYAD-211, for relapsed/refractory (r/r) multiple myeloma

  • Initial clinical activity observed, with one confirmed partial response (PR) observed in this low dose (30x106 cells per infusion)

Celyad Oncology SA (Euronext & Nasdaq: CYAD), a clinical-stage biotechnology company focused on the discovery and development of chimeric antigen receptor T-cell (CAR T) therapies for cancer, today announced that an abstract highlighting initial clinical data from the Phase 1 IMMUNICY-1 trial of CYAD-211 has been accepted for e-poster presentation at the upcoming European Hematology Association (EHA) Virtual Congress 2021

Filippo Petti, Chief Executive Officer at Celyad Oncology, commented, “We are very pleased with the initial results from the low dose cohort of our first shRNA-based allogeneic candidate, CYAD-211, which has showed preliminary signs of clinical activity, including a confirmed partial response, with no evidence of Graft-versus-Host-Disease. We are encouraged by the observed clinical activity at such a low dose level and the overall steady progress of the trial to date. Our team is intently focused on further assessing whether shRNA-mediated knockdown can generate safe, functional and clinically relevant allogeneic CAR T-cells for the treatment of cancer while offering an alternative technology platform with key advantages over gene-editing. We are excited for the opportunity to present the latest safety, clinical activity and cell kinetic data for the program next month at EHA and look forward to future updates for the program throughout 2021 as we move towards our goal of establishing proof-of-concept for this dynamic platform.”

The abstract published today is now available on the EHA 2021 website. Following the presentation at the meeting, the posters will be available in the Scientific Publications section of Celyad Oncology’s website.

Over 2B doses of COVID-19 vaccines to become available to India soon

 More than 2 billion doses of coronavirus vaccines will likely be available in India between August to December this year, a top government advisor said on Thursday.

Those doses would include 750 million of AstraZeneca's, vaccine, produced in India by the Serum Institute of India, as well as 550 million doses of Covaxin, made by Bharat Biotech, government advisor V K Paul told reporters at a news conference on Thursday.

Several Indian states are reporting an acute shortage of vaccines, even as coronavirus cases surge across the country.

https://news.yahoo.com/more-2-billion-doses-covid-115635053.html