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Monday, July 12, 2021

NRx, Quantum Leap Treat Severely Ill COVID-19 Patients with ZYESAMI

 NRx Pharmaceuticals, Inc. ("NRx") (Nasdaq: NRXP) and Quantum Leap Healthcare Collaborative (Quantum Leap) have begun treating patients with inhaled ZYESAMI(Aviptadil), in the I-SPY COVID Trial (NCT04488081), a phase 2 adaptive platform trial aimed at improving treatment for severely and critically ill COVID-19 patients.

The I-SPY COVID Trial utilizes Quantum Leap's adaptive platform trial design methodology, which focuses on the efficient assessment of multiple investigational agents simultaneously.

The objective of the trial is to screen a variety of promising agents for the treatment of severely and critically ill COVID-19 patients. Specifically, the goal is to identify agents that have a high impact on reducing mortality, as well as the need for and duration of mechanical ventilation.

ZYESAMI™ has demonstrated a statistically-significant increase in the likelihood of patients being alive and free of respiratory failure at 60 days when administered by intravenous infusion in a phase 2b/3 clinical trial in post-hoc analyses. In the I-SPY COVID Trial, inhaled ZYESAMI will be given to critically ill patients in order to determine whether inhaled administration has the potential to achieve similar results.

https://finance.yahoo.com/news/nrx-pharmaceuticals-quantum-leap-announce-124500992.html

CytoDyn advances leronlimab to Phase 2 for breast cancer

 CytoDyn Inc. (OTCQB: CYDY) ("CytoDyn" or the "Company"), a late-stage biotechnology company developing leronlimab, a CCR5 antagonist with the potential for multiple therapeutic indications, announced today its clinical trial with leronlimab in combination with carboplatin for the treatment of metastatic triple-negative breast cancer (mTNBC) has advanced from Phase 1b to a Phase 2 trial. The positive advancement confirms leronlimab will be administered with a 700 mg dosage for patients in the mTNBC trial and Basket trial for 22 solid tumor cancers, as well as compassionate use, eIND and “right-to-try” patients.

Scott Kelly, M.D., CytoDyn’s Chief Medical Officer and Chairman of the Board, commented, “In April of this year, we shared our early findings with the medical and scientific communities at the Triple Negative Breast Cancer Drug Development Digital Summit and the continued progress of our drug candidate, leronlimab. We believe these safety findings are a tremendous step forward for CytoDyn’s oncology program for all tumors that have the potential to be treated with leronlimab. Safety, quality of life, and toxicity are often the greatest concerns of oncology patients and these findings give great hope for those in need.”

https://www.bakersfield.com/ap/news/cytodyn-s-trial-for-metastatic-triple-negative-breast-cancer-demonstrates-safety-with-350-mg/article_cc2ca9f4-21de-56a1-be05-09aa9842b45a.html

Prothena sells amyloidosis portfolio to Novo Nordisk for up to $1.2B

 Shares of Prothena Corp. Plc PRTA, +7.28% were up 1.3% in premarket trading on Monday after the company announced a deal to sell its ATTR amyloidosis portfolio to Novo Nordisk NOVO.B, -0.18% in a $100 million deal that is worth up to $1.2 billion, based on milestones. ATTR amyloidosis is a rare disease that can cause a buildup of amyloid deposits in the body. One of the therapies in the portfolio is an experimental monoclonal antibody drug that has completed a Phase 1, open-label clinical trial. Prothena's stock has soared 393.2% so far this year, while the S&P 500 SPX, +1.13% is up 16.3%.

https://www.marketwatch.com/story/prothena-sells-amyloidosis-portfolio-to-novo-nordisk-for-up-to-12-billion-2021-07-12

Enochian: FDA Acceptance of Pre-IND Request For Potential Cure for Hepatitis B

 Enochian BioSciences, Inc., a company focused on gene-modified cellular and immune therapies in infectious diseases and cancer, today announced that the FDA has accepted a Pre-IND (Investigational New Drug) request for a potential cure of hepatitis B virus (HBV) infection. Written comments are expected this Fall.

The Pre-IND request was made based on promising data from a proof-of-concept study conducted in chimeric mice, considered by some scientific experts to be the ‘gold standard’ animal model to evaluate HBV cure.

Dr. Mark Dybul, a prominent expert in viruses and Executive Vice Chairperson of the Board of Enochian BioSciences, said, “As a long-time researcher, clinician, and leader of large global disease programs, I am very pleased that the FDA accepted our request to provide feedback to our Hepatitis B development program, and welcome the agency’s input. We are encouraged by the novel mechanism of action, called Hijack RNA that shows promise as a potential platform technology for coronaviruses (including the cause of COVID-19), influenza and HBV, and are exploring its use against HIV.”

https://finance.yahoo.com/news/enochian-biosciences-announces-fda-acceptance-110000334.html

KalVista: Oral KVD900 Significantly Slows Progression, Speeds Resolution of Attacks in HAE

 KalVista Pharmaceuticals, Inc. (NASDAQ: KALV), a clinical stage pharmaceutical company focused on the discovery, development, and commercialization of small molecule protease inhibitors, today announced data presented for its oral drug candidates at the European Academy of Allergy and Clinical Immunology (EAACI) Congress. Data presentations include a late-breaking poster for the Phase 2 data for KVD900, KalVista’s lead drug program for oral on-demand treatment of hereditary angioedema (HAE) attacks, two posters on the prevalence and clinical management of normal C1-INH HAE in the US, and two posters on the Company’s earlier stage research assets.

"HAE patients continue to seek an oral option for on-demand treatment of their disease, to fully manage their disease or for breakthrough attacks for those on prophylaxis," said Dr. Emel Aygören-Pürsün, Principal Investigator for the KVD900 Phase 2 Clinical Trial and Head of the HAE Center at the University Hospital Frankfurt. "As KVD900 halted attack progression and resolved attacks more quickly in patients with HAE, while demonstrating a good safety and tolerability profile, it could be a valued choice for physicians and patients in managing HAE."

The late-breaking poster, titled A single on-demand treatment with orally administered KVD900 significantly slows progression and accelerates resolution of attacks in patients with hereditary angioedema (HAE): results of a phase 2, placebo-controlled, double-blind cross-over trial, contains the comprehensive data set from the company’s Phase 2 clinical trial of KVD900 in HAE patients. The presented data supports the topline results reported in February 2021.

https://finance.yahoo.com/news/kalvista-pharmaceuticals-presents-data-showing-113100998.html

Janssen Gets U.S. FDA Approval of DARZALEX FASPRO Combo for Multiple Myeloma

 Halozyme Therapeutics, Inc. (NASDAQ: HALO) today announced that Janssen Biotech, Inc. (Janssen) received U.S. Food and Drug Administration (FDA) approval of DARZALEX FASPRO® (daratumumab and hyaluronidase-fihj) in combination with pomalidomide and dexamethasone (Pd) for the treatment of adult patients with multiple myeloma who have received at least one prior line of therapy, including lenalidomide and a proteasome inhibitor. The approval marks Janssen's sixth indication for DARZALEX FASPRO® in the treatment of multiple myeloma. Findings from the Phase 3 APOLLO study were recently published in The Lancet Oncology.

DARZALEX FASPRO® is co-formulated with recombinant human hyaluronidase PH20 (rHuPH20), Halozyme's ENHANZE® drug delivery technology.

https://www.wfmz.com/news/pr_newswire/pr_newswire_health/halozyme-announces-janssen-receives-u-s-fda-approval-of-darzalex-faspro-daratumumab-and-hyaluronidase-fihj/article_68029aa2-72b1-5d44-911e-80969c6481c4.html


Biogen Alzheimer’s drug clouds outlook for Medicare premiums next year

 The decision by U.S. drug regulators last month to approve a controversial treatment for Alzheimer’s disease could fuel an unusually large increase in Medicare premiums next year, but the outlook is clouded by a number of factors that will play out later this year.

Biogen Inc's drug Aduhelm could create hope for millions of older Americans afflicted with Alzheimer’s - if it is effective in combating the disease. But the U.S. Food and Drug Administration (FDA) approved the drug despite objections from its own scientific advisory panel, which voted nearly unanimously that clinical trials did not demonstrate its effectiveness.

Medicare typically covers FDA-approved drugs - but this one comes with an eye-popping price tag set by its maker - $56,000 per patient annually. That figure does not include other associated care that could add tens of thousands of dollars of additional costs.

Aduhelm will be administered by healthcare providers, and thus will be covered under Part B, rather than the Part D prescription drug program. And the impact on Part B finances could be huge. The premium paid by enrollees - which covers 25% of program costs - could rise sharply. So could the remainder of Part B costs, which are covered by all taxpayers.

Predicting actual costs is speculative at this point due to uncertainty about the number of patients Medicare decides should have access to Aduhelm. But even a conservative estimate of $29 billion annually, from the Kaiser Family Foundation https://bit.ly/3jUrSpM, would nearly double Part B spending on drugs, which totaled $37 billion in 2019. (https://bit.ly/3jUrSpM)

Medicare’s trustees will need to take into account the program’s likely spending on Aduhelm in 2022 as it sets the Part B premium, which typically is announced in November. And the new drug likely will have other impacts on the costs experienced by Medicare beneficiaries.

Many enrollees in traditional Medicare also have supplemental Medigap policies that cover their coinsurance costs. Premiums for those policies could rise as insurers anticipate higher outlays associated with Aduhelm. And 10% of traditional Medicare enrollees do not have supplemental coverage, so they would be subject to the program’s 20% cost-sharing requirement for Aduhelm - roughly $11,500 per year.

Out-of-pocket costs also would be an issue for enrollees in Medicare Advantage, the privately offered managed care alternative to the traditional program. Most Advantage enrollees are in plans that charge 20% coinsurance for Part B drugs provided in-network, mirroring the traditional program, according to Kaiser - the co-insurance rates can be much higher out of network.

Medicare typically covers FDA-approved drugs, but it can conduct its own reviews in order to decide which types of patients should be covered. In the case of Aduhelm, Medicare could limit use to patients in the early stages of Alzheimer's. Just last week, the FDA narrowed its own recommendation for prescription of the drug, saying it should be used only with patients who have mild cognitive impairment or early dementia.

Congress also could step in with legislation that mitigates any impact on Medicare enrollees. More broadly, the unusual FDA approval process and high cost for this drug could add fuel to the debate among legislators about broader drug-pricing reform.

“This gives credence to the argument that the pharmaceutical industry cannot be relied on to deliver value to patients,” said Rachel Sachs, a professor of law at Washington University in St. Louis who wrote about the Aduhelm controversy https://bit.ly/3hrAzX7 recently for the journal Health Affairs. (https://bit.ly/3hrAzX7)

OTHER PRESSURES

Two other factors could also put upward pressure on the Part B premium next year.

Medicare increased the Part B premium this year by just $3.90, to $148.50 per month. But the increase actually was on track to be larger - Congress stepped in to cap it at 25% of whatever it would have been if Medicare had followed the usual formula, as part of a COVID-19 relief bill. That could set the stage for a larger “catch-up” increase this year.

Healthcare utilization is another wild card. Despite the big surge in healthcare utilization last year associated with COVID-19, overall consumption of healthcare services fell dramatically during the lockdown last year. A key question is how this will impact utilization of services by Medicare enrollees next year. Utilization could be higher than normal as the pandemic recedes, putting further pressure on the Part B premium.

THE COLA FACTOR

The Aduhelm drama will play out against the backdrop of another pocketbook issue for seniors next year - the Social Security cost-of-living adjustment (COLA).

The recent surge in inflation has some forecasters predicting a very hefty COLA next year. The widely watched Consumer Price Index for All Urban Consumers (CPI-U) jumped 5% in May from a year earlier - the biggest gain since August 2008, when it rose 5.3%. The final COLA number will be decided by monthly data during the third quarter for the Consumer Price Index for Urban Wage Earners and Clerical Workers (CPI-W).

But for seniors who are enrolled in both Social Security and Medicare, the key figure is the net COLA after the Medicare Part B premium is deducted. Typically, some portion of the COLA is gobbled up by higher Part B premium costs. (The dollar amount of the Part B increase is deducted from the dollar amount of the COLA.)

Put it all together, and it could be a roller coaster ride this fall for seniors monitoring these pocketbook issues.

https://www.marketscreener.com/quote/stock/BIOGEN-INC-4853/news/Biogen-nbsp-New-Alzheimer-s-drug-clouds-outlook-for-Medicare-premiums-next-year-35835914/