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Thursday, March 4, 2021

Europe starts formal review of Russia's Sputnik V COVID-19 vaccine

 Europe’s medicines regulator said on Thursday it had started a rolling review of Russia’s Sputnik V COVID-19 vaccine, an important display of confidence in the shot that paves the way for its potential approval across the 27-nation bloc.

Hungary became the first EU country to grant the Russian vaccine emergency national approval in January, Slovakia has ordered shipments, and Czech Prime Minister Andrej Babis has said his country could move to use Sputnik V.

The European Medicines Agency (EMA) said in a statement it would review data from ongoing trials of the vaccine until there was enough evidence for a formal marketing authorisation application. (bit.ly/3uQxwfL)

EMA’s ‘rolling reviews’ are aimed at speeding up the approval process by allowing researchers to submit findings in real-time before final trial data is ready.

“While EMA cannot predict the overall timelines, it should take less time than normal to evaluate an eventual application because of the work done during the rolling review,” it said.

Kirill Dmitriev, CEO of the RDIF sovereign wealth fund that is promoting Sputnik V internationally, hailed the start of EMA’s rolling review as an important moment for Russia which he said showed its application had been a strong one.

“Sputnik V can act as a bridge between Russia and Europe, but its roll out should not get bogged down in politics,” Dmitriev told Reuters, praising Germany, France, Italy and Austria for what he called their pragmatic approach to Sputnik V.

The shot’s efficacy was initially greeted with scepticism by some Western scientists after Russia approved it in August last year without waiting for the results of full clinical trials.

However, some of those initial concerns appear to have faded after scientists said it was almost 92% effective in fighting COVID-19, based on peer-reviewed late-stage trial results published in The Lancet medical journal last month.

The two-shot vaccine uses two different weakened common cold viruses to deliver immune-building protein to the human body.

Dmitriev said Moscow could provide vaccines for 50 million Europeans starting from June if the shot won EU-wide approval, adding he expected several EU countries to approve the use of Sputnik V this month for their national use.

He did not name the countries.

Europe has so far approved vaccines from Pfizer/BioNTech, Moderna and AstraZeneca/Oxford, while ongoing reviews for CureVac and Novavax’s candidates are underway.

The EMA is expected to give its verdict on J&J’s single-shot vaccine on March 11.

https://www.reuters.com/article/us-health-coronavirus-europe-vaccines/europe-starts-formal-review-of-russias-sputnik-v-covid-19-vaccine-idUSKCN2AW0W8

Oncocyte expands access to DetermaRx

 Oncocyte Corporation (NYSE American: OCX), a molecular diagnostics company with a mission to provide actionable answers at critical decision points across the cancer care continuum, has signed an agreement with MultiPlan to participate in its networks. Through this agreement DetermaRx™ will now be available to those consumers with access to the PHCS and MultiPlan Network, MultiPlan’s national primary and complementary networks, at a pre-negotiated price per test. With more than one million healthcare providers participating in these networks and 60 million health plan members having access to MultiPlan’s services, this agreement significantly broadens the accessibility of Oncocyte’s proprietary treatment stratification test that identifies lung cancer patients with early stage non-squamous NSCLC who may benefit from adjuvant chemotherapy.

“Our agreement with MultiPlan underscores the recognition by the healthcare community of the important role DetermaRx plays in identifying lung cancer patients who are at high risk of recurrence, and whose survival rates can greatly benefit from receiving timely treatment,” said Padma Sundar, Chief Commercial Officer of Oncocyte. “MultiPlan’s partnership with hundreds of healthcare payors, along with its vast group of providers and plan members, will enable significantly expanded access to DetermaRx.”

https://www.globenewswire.com/news-release/2021/03/04/2187085/0/en/Oncocyte-Announces-Agreement-with-MultiPlan-Network-Expanding-Patient-Access-to-DetermaRx.html

Lipocine Publishes on Potential of LPCN 1144 in NASH, Hepatic Fibrosis

 Lipocine Inc. (NASDAQ: LPCN), a clinical-stage biopharmaceutical company focused on metabolic and endocrine disorders, today announced the publication of preclinical results supporting the therapeutic potential of LPCN 1144 in the treatment of and non-alcoholic steatohepatitis ("NASH") and hepatic fibrosis. The results were featured in a paper entitled "Treatment Potential of LPCN 1144 on Liver Health and Metabolic Regulation in a Non–Genomic, High Fat Diet Induced NASH Rabbit Model" (Comeglio et al), published in the Journal of Endocrinological Investigation (https://doi.org/10.1007/s40618-021-01522-7).

https://www.prnewswire.com/news-releases/lipocine-announces-publication-in-journal-of-endocrinological-investigation-highlighting-the-potential-of-lpcn-1144-in-the-treatment-of-nash-and-hepatic-fibrosis-301240212.html

Soligenix: Positive Progress in Pre-clinical Development of COVID-19 Vaccine

  Soligenix, Inc. (Nasdaq: SNGX) (Soligenix or the Company), a late-stage biopharmaceutical company focused on developing and commercializing products to treat rare diseases where there is an unmet medical need, announced today publication of pre-clinical immunogenicity studies for CiVax™ (heat stable COVID-19 vaccine program) demonstrating rapid-onset, broad-spectrum, neutralizing antibody and cell-mediated immunity is confirmed using full-length Spike protein antigens. The article titled, "Recombinant protein subunit SARS-CoV-2 vaccines formulated with CoVaccine HT adjuvant induce broad, Th1 biased, humoral and cellular immune responses in mice," has been posted as an accelerated preprint on bioRxiv (available here). This work will continue under a $1.5M Small Business Innovation Research (SBIR) grant awarded to Soligenix in December 2020.

CiVax™ is the Company's heat stable subunit vaccine candidate for the prevention of COVID-19, the infection caused by SARS-CoV-2. Ongoing collaborations with Axel Lehrer, PhD, Associate Professor in the Department of Tropical Medicine, Medical Microbiology and Pharmacology, John A. Burns School of Medicine (JABSOM), University of Hawaiʻi at Mānoa, have confirmed the feasibility of developing a broadly immunogenic vaccine for COVID-19. Using an efficient expression system in Drosophila S2 cells developed by Hawaii Biotech Inc., full-length Spike protein antigens have been produced and tested for immunogenicity in this latest work. These latest results demonstrate the immunogenic potential of the full-length CiVax™ antigen in combination with CoVaccine HT™, specifically in the context of SARS-CoV-2.

While a number of vaccines are available worldwide under Emergency Use Authorization, the requirement for cold chain shipping and timely administration, coupled with manufacturing scale up logistics, have limited the world's supply. Rapid vaccine administration worldwide is necessary to curtail disease spread and slow or pre-empt evolution of mutations, which may abrogate the effectiveness of current vaccine approaches. Previous work with the novel CoVaccine HT™ adjuvant, which Soligenix licensed from BTG Specialty Pharmaceuticals, a division of Boston Scientific Corporation, has indicated that CoVaccine HT™ can be thermostabilized both alone and in combination with antigens, potentially yielding a single vial presentation of the vaccine, which would not require cold chain distribution or storage.   

https://www.biospace.com/article/releases/soligenix-announces-positive-progress-in-the-pre-clinical-development-of-its-covid-19-vaccine/

Arbutus 2020 earnings, corporate update

AB-729, Arbutus’ proprietary subcutaneously delivered RNAi agent, demonstrates robust and continuous declines in hepatitis B surface antigen (HBsAg) in subjects with chronic hepatitis B (HBV) with favorable safety and tolerability data

Reductions in HBsAg seen in both HBV DNA negative and HBV DNA positive subjects support a potential dosing schedule for AB-729 as infrequently as every 8 to 12 weeks

Several AB-729 Phase 2 proof-of-concept combination clinical trials expected to initiate this year

AB-836, Arbutus’ proprietary oral capsid inhibitor, on track to begin a Phase 1a/1b clinical trial in healthy volunteers and subjects with HBV in the first half of 2021

Conference Call and Webcast Scheduled Today at 8:45 AM ET

Arbutus will hold a conference call and webcast today, Thursday, March 4, 2021 at 8:45 AM Eastern Time to provide a corporate update. You can access a live webcast of the call, which will include presentation slides, through the Investors section of Arbutus’ website at http://www.arbutusbio.com or directly at Live Webcast. Alternatively, you can dial (866) 393-1607 or (914) 495-8556 and reference conference ID 4084504.

An archived webcast will be available on the Arbutus website after the event. Alternatively, you may access a replay of the conference call by calling (855) 859-2056 or (404) 537-3406, and reference conference ID 4084504.

https://www.globenewswire.com/news-release/2021/03/04/2187007/0/en/Arbutus-Reports-Fourth-Quarter-and-Year-End-2020-Financial-Results-and-Provides-Corporate-Update.html

Dicerna: Roche Starts Phase 2 of Hep B Candidate Trial

 Dicerna Pharmaceuticals, Inc. (Nasdaq: DRNA) (the “Company” or “Dicerna”), a leading developer of investigational ribonucleic acid interference (RNAi) therapeutics, announced today that Roche has initiated RG6346 in a Roche-sponsored Phase 2 combination trial for the treatment of chronic hepatitis B virus (HBV) infection. RG6346 is an investigational GalXC™ RNAi therapeutic that Dicerna is developing in collaboration with Roche as part of the companies’ worldwide collaboration and licensing agreement for chronic HBV treatments. The Phase 2 platform trial will evaluate the efficacy and safety of RG6346 in combination with multiple additional agents with different mechanisms of action. Dicerna has earned a $25 million milestone in connection with the initiation of RG6346 in the Phase 2 combination trial.

The Roche Phase 2 trial (NCT04225715) is a randomized, adaptive, open-label platform trial designed to evaluate the safety, tolerability and efficacy of multiple combinations of novel agents in patients infected with chronic HBV against a common control, allowing rapid inclusion of additional treatment arms as needed. A combination of Roche’s novel investigational TLR7 agonist and core protein allosteric modulator (CpAM) inhibitor is currently already running within this study. In March 2021, RG6346 (also known as RO7445482) RNAi treatment arms have been initiated in combination with standard of care nucleos(t)ide (NUC) therapy and in triple combinations with Pegasys® (pegylated interferon alfa-2a), Roche’s CpAM inhibitor or Roche’s TLR7 agonist. The primary endpoint of the study is the percentage of participants with hepatitis B surface antigen (HBsAg) loss at 24 weeks after the end of the 48-week treatment period.

https://www.businesswire.com/news/home/20210304005276/en/Dicerna-Announces-Roche%E2%80%99s-Initiation-of-GalXC%E2%84%A2-RNAi-Candidate-RG6346-in-Phase-2-Combination-Trial-for-Treatment-of-Chronic-Hepatitis-B-Virus-Infection

Novartis to Make Up to 50 Million CureVac Covid Shots This Year

 Novartis AG agreed to produce CureVac NV’s Covid-19 vaccine candidate in a deal that will boost the potential supply of the shot by as much as 50 million doses this year.

The Swiss pharmaceutical giant could produce as many as 200 million doses next year, the partners said in a statement. Once the final agreement between the two is signed, Novartis plans to start production in the second quarter and ship the first deliveries to CureVac this summer.

Unlike Novartis’s previous agreement with BioNTech SE, which covered putting vaccines into vials, the CureVac deal is for producing and formulating the messenger RNA necessary to make the shot. Meanwhile, Novartis has more Covid production deals in the works, said Steffen Lang, head of the company’s technical operations.

“We have discussions on additional support for Covid vaccine manufacturers, but also for some of the therapeutic drugs which have the potential to be applied to treat Covid-19,” Lang said in an interview. “Rest assured that over the coming weeks we expect more news to be shared.”

Like the BioNTech shot, which is partnered with Pfizer Inc., CureVac’s experimental vaccine relies on mRNA technology to turn the body’s own cells into vaccine-making factories. The Tuebingen, Germany-based biotech has taken longer in the development process, however. Its shot is still in the final stage of clinical trials, with market approval expected in late May or June, Chief Executive Officer Franz-Werner Haas told European Union officials last week.

CureVac also has a cooperation pact with German drugs and chemicals maker Bayer AG. Bayer will help with regulatory clearances and global distribution and has said it expects to be able to produce 160 million doses of the vaccine next year at a factory in Wuppertal, Germany.

The Novartis production will be run in Kundl, Austria, a small town in the Alpine foothills. Scale-up will probably involve hiring 50 to 100 people, Lang said.

https://www.bloomberg.com/news/articles/2021-03-04/novartis-to-make-up-to-50-million-curevac-covid-shots-this-year