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Tuesday, April 6, 2021

Clear link between AZ vaccine and rare blood clots in brain: EMA official

 There is a link between AstraZeneca’s COVID-19 vaccine and very rare blood clots in the brain but the possible causes are still unknown, a senior official for the European Medicines Agency (EMA) said in an interview published on Tuesday.

“In my opinion we can now say it, it is clear that there is an association with the vaccine. However, we still do not know what causes this reaction,” Marco Cavaleri, chair of the vaccine evaluation team at the EMA, told Italian daily Il Messaggero when asked about the possible relation between the AstraZeneca shot and cases of brain blood clots.

Cavaleri added that the EMA would say there is a link although the regulator would not likely be in a position this week to give an indication regarding the age of individuals to whom the AstraZeneca shot should be given.

He did not provide evidence to support his comments.

AstraZeneca was not immediately available for comment. It has said previously its studies have found no higher risk of clots because of the vaccine.

The regulator has consistently said the benefits outweigh the risks as it investigates 44 reports of an extremely rare brain clotting ailment known as cerebral venous sinus thrombosis (CVST) out of 9.2 million people in the European Economic Area who have received the AstraZeneca vaccine.

The World Health Organization has also backed the vaccine.

The EMA said last week that its review had at present not identified any specific risk factors, such as age, gender or a previous medical history of clotting disorders, for these very rare events. A causal link with the vaccine is not proven, but is possible and further analysis is continuing, the agency said.

A high proportion among the reported cases affected young and middle-aged women but that did not lead EMA to conclude this cohort was particularly at risk from AstraZeneca’s shot.

The EMA is expected to give an update of its investigation on Wednesday.

Some countries, including France, Germany and the Netherlands, have suspending the use of the vaccine in younger people while the investigations continue.

Scientists are exploring several possibilities that might explain the extremely rare brain blood clots that occurred in individuals in the days and weeks after receiving the AstraZeneca vaccine.

European investigators have put forward one theory that the vaccine triggers an unusual antibody in some rare cases; others are trying to understand whether the cases are linked with birth control pills.

But many scientists say there is no definitive evidence and it is not clear whether or why AstraZeneca’s vaccine would cause an issue not shared by other vaccines that target a similar part of the coronavirus.

In a separate interview, Armando Genazzani, a member of the EMA’s Committee for Medicinal Products for Human Use (CHMP), told La Stampa daily that it was “plausible” that the blood clots were correlated to the AstraZeneca vaccine.

The AstraZeneca vaccine is based on a modified chimpanzee adenovirus vector, ChAdOx1, developed at Oxford University, and is one of several adenovirus-vector COVID-19 vaccines. The current vaccine rollout represents the first use of viral vector vaccines on such a global scale.

https://www.reuters.com/article/us-health-coronavirus-astrazeneca-vaccin/clear-link-between-az-vaccine-and-rare-blood-clots-in-brain-ema-official-tells-paper-idUSKBN2BT1ER

Molecular Partners: 1st Patient Dosed in a Phase 2 Trial of Ensovibep in COVID-19

 

  • First Study of Ensovibep in Patients With Symptomatic COVID-19 Disease
  • Designed To Evaluate Dynamics of Viral Clearance, Pharmacokinetics and Tolerability of Ensovibep
  • Ensovibep Is Additionally Planned To Be Tested in Two Global, Placebo Controlled, Double Blinded Trials: A Phase 2–3 Trial in an Ambulatory Patient Setting (Named EMPATHY), and a Phase 3 Trial in a Hospitalized Patient Setting Sponsored by the NIH (ACTIV-3)

Moderna, Catalent set long-term vax filling pact

 Moderna, Inc. (Nasdaq: MRNA), a biotechnology company pioneering messenger RNA (mRNA) therapeutics and vaccines, and Catalent, Inc. (NYSE: CTLT), the leading global provider of advanced delivery technologies, development, and manufacturing solutions for drugs, biologics, cell and gene therapies, and consumer health products, today announced the expansion of their strategic collaboration to dedicate a new high-speed vial filling line for the manufacture of the Moderna COVID-19 Vaccine and potentially other investigational programs in Moderna’s pipeline, at Catalent’s biologics facility in Bloomington, Indiana.

In June 2020, Catalent and Moderna announced that Catalent would provide aseptic vial filling and packaging from its Bloomington site, including additional staffing required for 24x7 manufacturing to support production of an initial 100 million doses of Moderna’s vaccine. On March 29, Moderna announced that this significant milestone was achieved.

As part of this expanded agreement, Catalent will now dedicate to Moderna’s use a new high-speed filling line at the site through June 2023, which can be used to manufacture the COVID-19 vaccine and potentially additional investigational programs in Moderna’s large clinical pipeline. Catalent will also provide inspection, labeling, cartoning, and final packaging for these programs.

"We appreciate this expanded collaboration with Catalent and the dedication of their team," said Juan Andres, Moderna’s Chief Technical Operations and Quality Officer. "This additional fill-finish capacity will be important for not only our COVID-19 vaccine, but also potentially for other programs in our clinical development pipeline."

"Catalent’s partnership with Moderna began in 2016, when we had only glimpsed the potential applications of mRNA and could not have guessed how pivotal mRNA would become in the fight against COVID-19," commented Alessandro Maselli, Catalent’s President and Chief Operating Officer. "We are proud to announce this extension of our companies’ strategic collaboration, and we look forward to further demonstrating our commercial manufacturing expertise as we help supply more vaccine doses."

Aptinyx Restarts Phase 2 Study of NYX-458 in Cognitive Impairment

 Patient screening has resumed following temporary suspension due to escalation of the COVID-19 pandemic

Data readout from the Phase 2 cognitive impairment study expected in 2H 2022

Three Phase 2 data readouts expected over the next 12 to 18 months across the company’s clinical development pipeline

Aptinyx Inc. (Nasdaq: APTX), a clinical-stage biopharmaceutical company developing transformative therapies for the treatment of brain and nervous system disorders, today announced that it has recommenced patient screening in a Phase 2 study of NYX-458 in patients with mild cognitive impairment and mild dementia associated with Parkinson’s disease and dementia with Lewy bodies. The company anticipates reporting data from this study in the second half of 2022.

https://finance.yahoo.com/news/aptinyx-recommences-phase-2-study-103700276.html

ANI Pharma to acquire Sandoz Inc. NDAs

 -- Accretive transaction in line with growth strategy laid out for Branded Products business --

ANI Pharmaceuticals, Inc. ("ANI") (NASDAQ:ANIP) today announced that it has acquired the new drug applications ("NDAs") for OXISTAT® Lotion, VEREGEN® Ointment, and Pandel® Cream and the abbreviated new drug application ("ANDA") for ApexiCon® E Cream from Sandoz Inc. Pandel® Cream will be transitioned later upon receiving the requisite approvals. Collectively, these products generated net revenues of $13.2 million in 2020. The acquisition was funded through borrowings under the Company’s pre-existing revolver credit facility.

In conjunction with the acquisition, ANI and Sandoz have entered into a multi-year manufacturing and supply agreement for OXISTAT® Lotion, Pandel® Cream and ApexiCon® E Cream. ANI intends to transfer the manufacture and packaging of these three products to its own manufacturing sites in the future.

"This acquisition is in line with our strategy to expand our established brands business through accretive deals. Importantly, ANI will ensure that patients in need continue to receive these high-quality dermatology products. The acquisition leverages our innovative brand commercialization infrastructure and our North American manufacturing footprint," stated Nikhil Lalwani, President and CEO.

The Company previously shared the four pillars of its strategy for delivering sustainable future growth:

  • Build a successful Cortrophin franchise;

  • Strengthen the Generics business by enhancing development capabilities and increased focus on niche opportunities;

  • Maximize the value from established brands through programmatic business development and innovative access and go-to-market strategies; and

  • Expand CDMO business leveraging unique North American-based manufacturing capabilities.

Valneva COVID Vax Candidate Using Dynavax Adjuvant

 


·5 min read

- VLA2001, an inactivated COVID-19 vaccine candidate with CpG 1018 adjuvant, was highly immunogenic and generally safe and well tolerated

-- 100% seroconversion rate for S-protein binding IgG antibodies in the high dose group

-- Neutralizing antibody titers at or above levels seen in convalescent sera

-- Majority of adverse events were mild to moderate

- Valneva plans to initiate a Phase 3 immunogenicity study in April 2021, subject to regulatory approval

https://finance.yahoo.com/news/positive-phase-1-2-results-100000668.html

EU expects to vaccinate majority by end-June

 Most European Union states will have enough COVID-19 vaccines to immunize the majority of their people by the end of June, Bloomberg News reported on Tuesday, citing an internal memo.

Germany, France, Italy, Spain and the Netherlands will be in a position to fully inoculate more than 55% of their populations by June end, the report https://www.bloomberg.com/news/articles/2021-04-06/eu-will-near-virus-immunity-by-end-june-internal-memo-shows?sref=SCAzRb9t added, citing projections in the memo by the EU executive, the European Commission.

The numbers confirm public estimates of vaccines the 27-nation bloc expects to receive in the second quarter.

The Commission has repeatedly said the EU, with a population of nearly 450 million, is to receive about 360 million doses by the end of June in addition to about 100 million already shipped.

That would be sufficient to meet its target of vaccinating at least 70% of the bloc's adult population by the summer.

The bloc expects to receive in the April-June period 55 million doses of the single-dose vaccine developed by Johnson & Johnson, and another 300 million of two-dose shots from BioNTech-Pfizer , AstraZeneca and Moderna.

It is however unclear whether all expected doses will be delivered in line with timetables. The EU received about half of the expected doses in the first quarter because AstraZeneca made major cuts in its supplies to the EU then.

The new estimates already factor in a further major cut in AstraZeneca supplies in the second quarter.

The EU has coordinated the purchase of vaccines with EU governments but has no power on vaccination plans, which are run by EU states.

Roll-outs depend on supplies but also on vaccination programmes, which have often been hampered in EU states because of safety and effectiveness concerns over the AstraZeneca vaccine.

The vaccine roll-out picked up in the bloc at the end of March after a slow start.

https://www.marketscreener.com/quote/stock/ASTRAZENECA-PLC-120960697/news/EU-expects-to-vaccinate-majority-by-end-June-Bloomberg-32892223/