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Thursday, April 30, 2020

Glenmark to conduct trials in India for potential COVID-19 drug

Glenmark Pharmaceuticals Ltd (GLEN.NS) said on Thursday it will start clinical trials in India of antiviral drug favipiravir, seen as a potential treatment for COVID-19, sending its shares up as much as 9%.
The trials come after a Chinese official told reporters last month that an active ingredient of the drug had been effective, with no obvious side effects, in helping coronavirus patients recover.
Favipiravir is manufactured under the brand name Avigan by a unit of Japan’s Fujifilm Holdings Corp (4901.T) and approved for use as an anti-flu drug in the country in 2014.
Mumbai-based Glemark said the approval made it the first pharmaceutical company in India to be given the go-ahead to start trials on COVID-19 patients in the country, which recorded its 1,000th coronavirus-related death on Wednesday.
“After having successfully developed the API (active pharmaceutical ingredient) and the formulations … Glenmark is all geared to immediately begin clinical trials on favipiravir on COVID-19 patients in India,” Sushrut Kulkarni, executive vice-president for global R&D, Glenmark Pharmaceuticals, said in a statement reut.rs/2VNF43h.
Drugmakers across the world have been rushing to develop a treatment or vaccine for the fast-spreading coronavirus that has killed over 220,000 people and ravaged financial markets.
Early clinical trial results on Wednesday from Gilead Sciences Inc’s (GILD.O) experimental antiviral drug remdesivir showed it helped patients recover more quickly from the illness caused by the coronavirus.
Glenmark will initially enroll 150 patients with mild-to-moderate COVID-19 in a randomized trial that will compare favipiravir with standard supportive care. The trial will last for a maximum of 28 days, it said.
The Drug Controller General of India, which approved the trials, declined to provide more detailed information.
Another Indian pharmaceutical company, Strides Pharma Science Ltd (SRID.NS), said on Wednesday it had developed and commercialized favipiravir antiviral tablets, and had applied to the authorities to start trials.
https://www.reuters.com/article/us-glenmark-pharms-stocks/glenmark-to-conduct-trials-in-india-for-potential-covid-19-drug-idUSKBN22C0IZ

Vaxart up on encouraging data on oral COVID-19 vaccine candidates

Vaxart (NASDAQ:VXRT) is up 15% premarket on robust volume in reaction to its announcement of positive preclinical data on its oral COVID-19 vaccine candidates, several of which generated immune responses in all tested animals after a single dose.
CSO Sean Tucker, Ph.D., says, “These preclinical results confirm that all constructs are immunogenic as measured by IgG antibodies in serum and we observed a robust boosting effect after the second dose. This latest data set will help to select the lead candidate for manufacturing and we remain on track to start a first phase 1 study in the second half of this year.”
Orally administered vaccines, while preferable to the injected variety assuming comparable immunogenicity, have always been more challenging to develop due to the harsh conditions in the human digestive tract.
https://seekingalpha.com/news/3566947-vaxart-up-15-premarket-on-encouraging-data-on-oral-covidminus-19-vaccine-candidates

Jazz Pharma comes up empty in late-stage defibrotide study

Jazz Pharmaceuticals (NASDAQ:JAZZ) slips 3% premarket on light volume on the heels of disappointing results from a Phase 3 clinical trial evaluating defibrotide for the prevention of hepatic veno-occlusive disease (VOD) after hematopoietic stem-cell transplantation (HSCT) in high-risk or very high-risk patients.
Enrollment was stopped early after the independent Data Monitoring Committee concluded that the study was unlikely to meet the primary endpoint based on an interim analysis of data on the first 280 participants.
The company says it will stop development for the indication but will stay the course in other studies.
The FDA approved defibrotide, branded as Defitelio, in March 2016 for the treatment of hepatic VOD after HSCT.
https://seekingalpha.com/news/3566968-jazz-pharma-comes-up-empty-in-late-stage-defibrotide-study

NovoCure EPS beats by $0.02, misses on revenue

NovoCure (NASDAQ:NVCR): Q1 GAAP EPS of $0.04 beats by $0.02.
Revenue of $101.83M (+38.9% Y/Y) misses by $0.27M.
https://seekingalpha.com/news/3566663-novocure-eps-beats-0_02-misses-on-revenue

Syneos Health EPS beats by $0.04, beats on revenue

Syneos Health (NASDAQ:SYNH): Q1 Non-GAAP EPS of $0.68 beats by $0.04; GAAP EPS of $0.32 beats by $0.15.
Revenue of $1.16B (+3.6% Y/Y) beats by $20M.
https://seekingalpha.com/news/3566707-syneos-health-eps-beats-0_04-beats-on-revenue

AstraZeneca teams up with Oxford U. on COVID-19 vaccine

AstraZeneca (NYSE:AZN) will collaborate with the University of Oxford on the development and distribution of the latter’s recombinant adenovirus vaccine candidate, ChAdOx1 nCoV-19, for the prevention of COVID-19 infection.
Phase 1 studies commenced last week in healthy volunteers with results expected next month. Later stage trials should launch mid-year.
The vaccine is designed to generate a strong immune response from a single dose.
Shares up 4% premarket on light volume.
https://seekingalpha.com/news/3566711-astrazeneca-teams-up-oxford-u-on-covidminus-19-vaccine

CytoDyn reports ‘strong results’ with leronlimab in COVID-19

CytoDyn (OTCQB:CYDY) announces results from 49 U.S. COVID-19 patients who received CCR6 antagonist leronlimab under emergency use authorization. Highlights:
11 patients in ICUs in New York with acute respiratory care, eight on mechanical ventilation. Seven died and four survived. The data have been submitted for publication tomorrow.
23 patients in Southern California, six in critical condition and intubated and 17 severely ill on oxygen support. Three of the six were taken off ventilators, two were stable and one deteriorated. 11 of the 17 showed improvement in respiratory parameters and eight were discharged from the hospital, two were stable, two deteriorated and status unknown on two others.
Three patients in Georgia, all were in ICUs and intubated. Two were taken off ventilators while one remains but is improving.
A NY patient on oxygen support was discharged from the hospital while another in Northern CA was weaned off ventilation and transferred to a rehab hospital.
Enrollment in a Phase 2 study and a Phase 2b/3 trial is “moving rapidly.”
https://seekingalpha.com/news/3566728-cytodyn-reports-strong-results-leronlimab-in-covidminus-19