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Tuesday, March 1, 2022

Gilead Hit By FDA Complete Response Letter For Lenacapavir In HIV Infection

 

  • The FDA has issued a complete response letter (CRL) for Gilead Sciences Inc's  (Get Free Alerts for GILD) application for lenacapavir for heavily treated multi-drug resistant (MDR) HIV-1 infection.
  • Lenacapavir is an investigational, long-acting HIV-1 capsid inhibitor.
  • In the CRL, the FDA has cited Chemistry Manufacturing and Controls (CMC) issues relating to the compatibility of lenacapavir with the proposed container vial. 
  • The FDA raised questions about vials made of borosilicate glass and their compatibility with the lenacapavir solution, resulting in a clinical hold for injectable lenacapavir.
  • Gilead intends to provide FDA with a comprehensive plan and corresponding data to use a different vial type.
  • The lenacapavir application was submitted to the FDA to treat heavily-treatment experienced people with multi-drug resistant HIV in June 2021 and selected for priority review. 

Pfizer's Clostridioides Difficile Vaccine Fails To Prevent Infection

 

  • Pfizer Inc  (Get Free Alerts for PFE) announced data from the CLOVER Phase 3 trial evaluating Clostridioides difficile vaccine candidate to prevent C. difficile infection (CDI).
  • Initial analyses of two secondary endpoints indicated a highly favorable benefit in reducing CDI severity and 100% vaccine efficacy in preventing medically attended CDI.
  • However, the trial did not meet its pre-specified primary endpoint of prevention of primary CDI. 
  • Safety reviews indicated that the investigational vaccine was safe and well-tolerated.
  • Vaccine efficacy under the primary endpoint was 31% following the third dose and 28.6% following the second dose for the C. difficile vaccine candidate. 
  • For all CDI cases recorded 14 days post dose 3, vaccine efficacy 49%, 47%, and 31% up to 12 months, 24 months, and at the final analysis, respectively.
  • Pfizer noted a highly favorable potential benefit in reducing the duration and severity of the disease. 
  • None of the participants with CDI in the vaccine group required medical attention (including hospitalization) compared to 11 in the placebo group. 

Lower Vascepa Volume Hits Amarin's Q4 Topline Growth

 Amarin Corp plc's 

 (Get Free Alerts for AMRN) Q4 FY21 sales decreased 13.6% Y/Y to $144.49 million, beating the consensus of $141.75 million.

  • The decline was driven primarily by the volume of Vascepa sales adversely impacted by the generic icosapent ethyl market entrants and the ongoing challenges of the COVID-19 pandemic.
  • The cost of goods sold was $30.63 million, compared to $34.76 million. Amarin's overall gross margin on net product revenue was 79.2%, compared with 79.9% a year ago.
  • SG&A expense was $92.36 million compared to $116.82 million in the prior year, primarily due to a decrease in marketing and direct-to-consumer promotions in 2021 due to the impact of COVID-19 and the company's focus on improving the profitability of operations.
  • The decrease also includes reducing costs associated with the company's Go-To-Market strategy, resulting in decreased promotional initiatives, reduced travel, and decreased sales force.
  • The company reported adjusted EPS of $0.06 compared to $0.04 a year ago and the consensus of $(0.02).
  • Amarin held aggregate cash and investments of $489.1 million at the end of 2021.
  • Guidance: Amid uncertainty related to the impact of COVID-19 and generic availability, Amarin is unable to provide 2022 revenue guidance.

CTI BioPharma's Bone Marrow Cancer Drug Scores FDA Approval

 

  • The FDA approved CTI BioPharma Corp's  (Get Free Alerts for CTIC) Vonjo (pacritinib) for treating adult patients with myelofibrosis, a type of bone marrow cancer with low blood platelets count.
  • Pacritinib is a JAK inhibitor and will compete with Incyte Corporation's  (Get Free Alerts for INCY) Jakafi and Bristol Myers Squibb's Co  Inrebic, which were approved in 2011 and 2019, respectively for myelofibrosis.
  • CTI BioPharma Chief Executive Officer Adam R. Craig said, "We are fully funded for commercial launch, following our debt and royalty transactions with DRI, and we look forward to providing VONJO to patients within 10 days."
  • The Company said the drug was approved under priority, and the nod triggered a $60 million payment from DRI Healthcare Trust.
  • The accelerated approval is based on efficacy results from the pivotal Phase 3 PERSIST-2 study. 
  • Pacritinib 200 mg twice daily showed 29% of patients had a reduction in spleen volume of at least 35% compared to 3% of patients receiving the best available therapy, including Jakafi (ruxolitinib). 
  • As part of the accelerated approval, CTI must describe a clinical benefit in a confirmatory trial. CTI plans to complete the PACIFICA trial to fulfill this post-approval requirement, with expected results in mid-2025.
  • In November, the agency had delayed its decision for the drug by three months to review additional data previously submitted by the Company.

FDA approves cancer therapy by J&J, partner Legend

 The U.S. health regulator has approved a therapy developed by Johnson & Johnson and its China-focused partner Legend Biotech Corp to treat a type of white blood cell cancer, the U.S. healthcare company said on Monday.

The Food and Drug Administration's decision paves the way for Legend's first approved product in the United States, at a time when the regulator has stepped up its scrutiny of drug trials conducted in China. The Legend-J&J therapy was tested initially in China, and then in the United States and Japan.

"This is the first of many cell therapies we plan to bring to patients as we continue advancing our pipeline across disease states," said Ying Huang, Legend's chief executive officer and chief financial officer.

The treatment, Carvykti/Cilta-cel, belongs to a class of drugs known as CAR-T therapies, or chimeric antigen receptor T-cell therapies.

CAR-T drugs work by harvesting a patient's own disease-fighting T-cells, genetically engineering them to target specific proteins on cancer cells, and replacing them to seek out and attack cancer.

Legend and J&J will sell the drug in Greater China at 70-30 split in profit, and in all other countries in a 50-50 split in profit. https://bit.ly/3C1cfns

A decision on the CAR-T therapy was initially expected to come by the end of November after it was given priority review six months earlier, but this was extended by three months to allow sufficient time to review information submitted by J&J following an FDA request.

Legend, which initiated the development, signed an agreement with Janssen Biotech Inc, an arm of J&J, in 2017, to jointly develop and commercialize the drug, with Legend getting $350 million in upfront payment.

Besides the United States, Carvykti/Cilta-cel is also being reviewed by health authorities in Japan and Europe. A Marketing Authorisation Application (MAA) for the therapy in China is yet to be filed. 

https://finance.yahoo.com/news/1-fda-approves-cancer-therapy-021427562.html

Pfizer Covid vaccine is less effective in kids 5 to 11, study finds

 Newly emerging data suggest the Pfizer-BioNTech Covid vaccine works substantially less well at preventing infection and hospitalizations in children aged 5 to 11 than it does in those aged 12 to 17 — a finding that is raising questions about whether the companies chose the wrong dose for the younger children.

The data, from New York state, show a rapid and substantial decline in protection after vaccination in children in the younger age group, with efficacy against infections dropping off more quickly and dramatically than the declines seen in children aged 12 to 17. The study also found a significant, but less steep, decline in protection against hospitalizations.

The findings, compiled by researchers working for the New York State Department of Health, were posted Monday on a preprint server; the study has not yet undergone peer review.

The New York findings, along with data from several other databases, were recently presented to the Covid vaccine work group of the Advisory Committee on Immunization Practices, independent vaccine experts who advise the Centers for Disease Control and Prevention, sources told STAT.

The data come on the heels of disappointing results from Pfizer trials of an even lower vaccine dose in children under the age of 5. And they will raise questions about whether, in trying to find doses that were both protective and tolerable in children, the companies failed to hit the mark for both age groups.

Pfizer would not say if it is exploring the possibility that the dose used in children might be too low, but said it is “confident in the protection and safety” of its Covid-19 vaccine.

“Our updates earlier this year on pursuing a 3-dose schedule for the pediatric population were informed by the effectiveness data for three doses of the vaccine for people 16 years and older, and the early laboratory data observed with Delta and other variants of concern, including Omicron, which suggest that people vaccinated with three doses of a Covid-19 vaccine may have a higher degree of protection,” it said in an emailed statement.

But John Moore, a virologist at Weill Cornell Medical College, said given the findings of this study, it’s hard to see how the lower efficacy in children aged 5 to 11 could be due to anything but the lower dose they received. In the study, children aged 12 had the highest vaccine efficacy of all age groups in both cohorts.“The striking difference between 11- and 12-year-olds can only be explained by the three-fold dosing reduction in the younger children. The one-year age difference is highly unlikely to make any other factor relevant,” Moore said by email. “The 11-year-olds got the 3-fold reduced dose, the 12-year-olds the standard dose.”

The New York study analyzed health records for Covid cases in children and teens from Dec. 13, 2021 to Jan. 30, 2022, a period during which the Omicron variant was fast replacing all other forms of the SARS-CoV-2 virus in the country. Covid vaccines are not as protective against Omicron as they were against earlier versions of the virus, especially without a booster shot.

The state recorded more than 850,000 Covid cases in adolescents aged 12 to 17 during that time, and about 365,000 in children aged 5 to 11.

Over that period, two-dose vaccine protection against infection for kids aged 5 to 11 declined from 68% to 12%; the vaccine’s effectiveness at preventing hospitalization declined from 100% to 48%.

But two-dose protection against infection for children aged 12 to 17 only dropped from 66% to 51%, and protection against hospitalization from 85% to 73%.

“Our data support vaccine protection against severe disease among children 5-11 years, but suggest rapid loss of protection against infection, in the Omicron variant era,” the researchers wrote. “Should such findings be replicated in other settings, review of the dosing schedule for children 5-11 years appears prudent.”

The adult Pfizer regimen — used in anyone aged 12 and older — is two doses of 30 micrograms apiece, given 21 days apart. Children 5 to 11 years old receive a dose that is one-third that size, two doses of 10 micrograms apiece. And in studies of children under 5, the dose is further reduced, with the children aged 6 months to 4 years getting two 3-microgram doses. The vaccine is not yet authorized for use in children under 5.

In December, Pfizer announced that two doses of the vaccine in children under 5 had not generated the same level of antibodies as was seen after two doses in people 16 to 25, which was being used as a proxy for protection. It said it would give the children under 5 a third dose to see if that achieved the required level of protection.

But then as Omicron cases spiked across the country, the Food and Drug Administration revealed it was considering a rolling authorization for the vaccine for children under age 5, allowing parents to start vaccinating their children while waiting for the third dose. The rationale was that the risk-benefit equation had shifted with Omicron.

A meeting of the FDA’s vaccine advisers, the Vaccines and Related Biological Products Advisory Committee, was scheduled for mid-February. But before the group could meet the FDA and Pfizer announced the plan was on hold. The plan is now to wait for the third-dose results before considering authorization in this age group.

https://www.statnews.com/2022/02/28/pfizer-covid-vaccine-kids-5-11/

New Mexico bill allows testing to prevent fentanyl deaths

 New Mexico is allowing broad access to test strips that can detect the presence of the potent opiate fentanyl and potentially help avoid deadly overdoses, under legislation signed Monday by Democratic Gov. Michelle Lujan Grisham.

The bill from Democratic legislators in Albuquerque, Santa Fe and Los Alamos lifts restrictions on public access to devices that can test for drug impurities. It also gives state health health officials new authority to intervene and rein in the spread of diseases like HIV and hepatitis that can be transmitted through intravenous drug use.

Overdoses in New Mexico increasingly are linked to the ingestion of drugs laced with fentanyl. States including Arizona already have decriminalized test strips designed to detect fentanyl.

New Mexico routinely leads the American West in rates of opioid-related drug overdose deaths. It also has been on the forefront of strategies to reduce the toll of drug use and addiction, from the distribution of overdose antidote drugs to legal immunity provisions for people who may implicate themselves in crimes by seeking overdose treatment for themselves or others.

https://apnews.com/article/business-health-new-mexico-albuquerque-santa-fe-dc44c1be7a0657580cfb1f17c2c9de44