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Friday, September 18, 2020

Immunomedics antibody-drug conjugate shows promise v. brain tumors

Immunomedics (NASDAQ:IMMU) announces encouraging Phase 1 data on antibody-drug conjugate Trodelvy (sacituzumab govitecan) (formerly IMMU-132) in patients with brain tumors. The results were virtually presented at ESMO.

At data cutoff, 19 patients were enrolled in the single-center study, 12 with recurrent glioblastoma multiforme (rGBM), the most aggressive type of brain cancer, and seven with brain metastatic breast cancer (BMBC).

Trodelvy delivered 150-fold and 40-fold the 50% inhibitory concentration (IC50) of SN-38, the cytotoxic payload, for BMBC and rGBM, respectively, and produced partial responses in both cohorts.

Progression-free survival (ongoing) was 161-279 days in four BMBC patients and 7-315 days in six rGBM patients.

No new safety signals were observed.

https://seekingalpha.com/news/3615303-immunomedics-antibody-drug-conjugate-shows-encouraging-action-in-brain-tumors

European advisory group backs Roche’s Tecentriq in first-line liver cancer

The European Medicines Agency’s advisory group CHMP has adopted a positive opinion backing the use of Roche’s (OTCQX:RHHBY +1.4%) Tecentriq (atezolizumab), combined with Avastin (bevacizumab), for the treatment of adults with advanced or unresectable hepatocellular carcinoma in a first-line setting.

The PD-L1 inhibitor is currently approved in Europe for the treatment of urothelial, non-small cell lung, small cell lung and breast cancers.

A final decision from the European Commission usually takes ~60 days.

https://seekingalpha.com/news/3615348-european-advisory-group-backs-roches-tecentriq-in-first-line-liver-cancer

New restrictions across Europe as COVID-19 cases rise dramatically

Targeted lockdowns and local restrictions are returning to Europe as the region tries to avoid broad economic damage amid a surge in coronavirus cases.

“Weekly cases have now exceeded those reported when the pandemic first peaked in Europe in March,” the WHO’s regional director for Europe Hans Kluge told an online news conference. “Although these numbers reflect more comprehensive testing, it also shows alarming rates of transmission across the region.”

Pubs and restaurants must shut early and household mixing has been limited in northeast England, while social gatherings of more than six people have been banned across the country.

French authorities are meanwhile preparing tighter restrictions in several cities, while Spain’s Madrid has moved to “reduce mobility and contacts” in areas with high infection rates.

Outside Europe, Israel is set to be the first developed country to enforce a second nationwide shutdown, which will begin later this afternoon.

https://seekingalpha.com/news/3615217-new-restrictions-across-europe-covidminus-19-cases-rise-dramatically

Thursday, September 17, 2020

China’s Sinovac to test coronavirus vax candidate in teenagers, children

Chinese vaccine maker Sinovac Biotech plans to start a clinical trial of its experimental coronavirus vaccine with children and adolescents later this month, widening its test on a shot that’s already in the final stage of study with adults.

Finding a vaccine that works for the entire population, including younger people, could be crucial to preventing outbreaks of the virus – that has led to over 930,000 deaths worldwide – through schools and kindergartens, potentially affecting also teachers and parents.

A total of 552 healthy participants aged between three and 17 will take two doses of U.S.-listed Sinovac’s CoronaVac or a placebo in a combined Phase 1 and Phase 2 trial estimated to begin on Sept. 28 in the northern Chinese province of Hebei, according to a registration record https://bit.ly/35JkYgf published on Wednesday.

The trial has already approved by Chinese regulator, a Sinovac spokesperson said.

China has inoculated at least tens of thousands of its citizens rolling out experimental coronavirus vaccines, attracting international interest in their development, despite expert concerns over the safety of drugs that have not completed standard testing.

As part of that programme, CoronaVac, being tested in final-stage large-scale trials in Brazil, Indonesia and Turkey, has already been given to about 90% of the company’s employees and their families.

Data so far suggests the virus generally causes milder disease in children compared with adults, but some cases of children requiring intensive care have been also reported, according to the World Health Organization.

Several hundred children were admitted to U.S. hospitals with a rare but severe inflammatory syndrome, which could include symptoms such as fever, rashes and swollen glands, associated with the coronavirus.

Sinovac said earlier this month CoronaVac appeared to be safe and able to induce antibodies for older people, while the vaccine-generated antibody levels were slightly lower than seen in younger adults, citing preliminary results from an early to mid-stage trial.

https://www.marketscreener.com/quote/stock/SINOVAC-BIOTECH-LTD-5714593/news/Sinovac-Biotech-China-s-Sinovac-to-test-coronavirus-vaccine-candidate-in-teenagers-children-31310420/

Alibaba Health, Sinovac partner on virus inoculation platform

China’s Sinovac Biotech has partnered with Alibaba Health Information Technology to build a platform for people to book inoculation with a potential coronavirus vaccine, the company said on Thursday.

The two firms signed a strategic pact about the platform, which will also offer services such as follow-up checks after vaccinations and proof of vaccination, Sinovac said on China’s WeChat social media.

At the moment, access to the platform is limited to those at high risk of infection, such as medical workers eligible for an emergency use program that China launched in July, Sinovac said.

Access might be widened when the vaccine is ready for public use, a spokesman added.

Tens of thousands of people have already received its vaccine candidate CoronaVac, which is in final-stage large-scale trials in Brazil, Indonesia and Turkey, via the emergency use vaccine.

About 90% of the firm’s employees and their families are participating in the emergency use program.

https://www.marketscreener.com/quote/stock/ALIBABA-HEALTH-INFORMATIO-6165753/news/Alibaba-Health-Sinovac-partner-on-virus-inoculation-platform-31311789/

U.S. plans for hundreds of millions of cheap, fast COVID-19 tests

U.S. manufacturers are sharply increasing production of cheap, fast – but less accurate – COVID-19 tests, aiming for 100 million per month by year end that will enable schools and workplaces to significantly expand testing.

Manufacturing and government sources tell Reuters that more than half a dozen so-called antigen tests will likely be authorized by the end of October. U.S. regulators in recent months have authorized antigen tests from Abbott Laboratories, Becton Dickinson & Co, Quidel Corp and LumiraDX.

When planned production of the newly authorized tests are combined with previously approved diagnostics, overall monthly U.S. testing capacity will exceed 200 million per month by year end, these sources said.

Makers of the four recently-approved antigen tests have the capacity to make around 40 million per month, but expect to more than double that by year end, according to a Reuters analysis that includes proprietary figures shared by companies.

Unlike the $100 and up molecular diagnostics currently dominating U.S. testing that must be sent to a lab and often take several days for results, antigen tests can cost as little as $5. They can be performed anywhere and produce results in minutes.

That opens the possibility of regular screening at schools and businesses of even asymptomatic people, an important tool for containing future outbreaks, experts said.

“If we could get testing to a scale where everyone you want to test can be tested quickly and cheaply with a quick turnaround time (for results), then you could screen people” before they spread the virus, said Dwayne Breining, director of labs at Northwell Health, New York state’s largest hospital system.

Lab-based molecular tests are too hard to make and deploy at that level, he said.

Antigen tests detect certain proteins that are part of the virus from samples taken via nasal or throat swabs, similar to rapid tests for strep throat in a doctor’s office.

RELIABILITY CONCERNS

A lack of testing capacity and little federal coordination early in the pandemic hampered efforts to control spread of the virus that has infected more than 6 million people in the United States.

Still, regulators and health experts are concerned about antigen test reliability. They typically detect the virus around 80% to 90% of the time, below the more than 95% rate of lab-based tests. False negative results raise the likelihood that sick people could unwittingly spread COVID-19.

There is also not enough data to be certain the new tests can detect the virus when infected people are in the early, pre-symptomatic stage, potentially limiting their usefulness.

The U.S. conducted around 25 million tests in August, including lab and antigen tests, according to data from the University of Oxford. Antigen test makers and their suppliers are gearing up for a huge boost.

Tony Lemmo, chief executive of BioDot Inc, which makes dispensers of chemicals used in the tests, says he has recently received orders that would translate into some 500 million tests in the coming months.

The United States could have capacity to conduct 3 million coronavirus tests per day this month, about half of them antigen tests. That could climb to as high as 135 million monthly tests in October, a top health official told a U.S. congressional panel on Wednesday.

European diagnostics companies Roche Holding AG and Quiagen NV have said they will apply for U.S. authorization for their antigen tests.

The National Institutes of Health is working with companies on new tests that will likely add as many as another 30 million tests per month to overall capacity this year, a U.S. official told Reuters. The agency has also provided grants to help testmakers boost manufacturing capacity, including $71 million to Quidel in July.

The U.S. official, who was not authorized to speak publicly, told Reuters that getting to 100 million tests a month by year end could potentially slip by a couple of months because of production challenges.

To ramp up, companies need to hire enough skilled workers and source the paper used in the tests, called nitrocellulose, the official said.

“There’s just so much required to go from zero to millions of tests,” said Quidel CEO Douglas Bryant, whose company is working with large U.S. universities on daily testing of student athletes.

College football teams in the Big Ten conference will use antigen testing after announcing on Wednesday they would go ahead with games beginning next month.

Nursing homes are using Becton Dickinson’s antigen tests to screen residents and staff through a government program.

Even if testmakers succeed in scaling production, capacity will remain tight for some time, as schools, employers and others clamor for tests, executives and officials said.

Quidel has prioritized customer requests for its tests, Bryant said, with healthcare facilities and schools near the top, and industries like tourism further back in line.

https://www.marketscreener.com/quote/stock/QUIDEL-CORPORATION-10595/news/U-S-plans-for-hundreds-of-millions-of-cheap-fast-COVID-19-tests-31312986/

Methylprednisolone for hospitalised severe Covid-19 patients: randomised controlled clinical trial

Maryam Edalatifard, Maryam Akhtari, Mohammadreza Salehi, Zohre Naderi, Ahmadreza Jamshidi, Shayan Mostafaei, Seyed Reza Najafizadeh, Elham Farhadi, Nooshin Jalili, Masoud Esfahani, Besharat Rahimi, Hossein Kazemzadeh, Maedeh Mahmoodi Aliabadi, Tooba Ghazanfari, Mohammad Reza Satarian, Hourvash Ebrahimi Louyeh, Seyed Reza Raeeskarami, Saeidreza Jamali Moghadam Siahkali, Nasim Khajavirad, Mahdi Mahmoudi, Abdorahman Rostamian

European Respiratory Journal 2020;

DOI: 10.1183/13993003.02808-2020

PDF: https://erj.ersjournals.com/content/erj/early/2020/09/09/13993003.02808-2020.full.pdf

Abstract

Background There are no determined treatment agents for the severe coronavirus disease 2019 (COVID-19); therefore, it is suggested that methylprednisolone, as an immunosuppressive treatment, can reduce the inflammation of the respiratory system.

Methods We conducted a single-blind, randomised, controlled, clinical trial involving severe hospitalised patients with confirmed COVID-19 at the early pulmonary phase of the illness in Iran. The patients were randomly allocated in a 1:1 ratio by block randomisation method to receive standard care with methylprednisolone pulse (intravenous injection, 250 mg·day−1 for 3 days) or standard care alone. The study endpoint was the time of clinical improvement or death, whichever came first. Primary and safety analysis was done in the intention-to-treat (ITT) population.

Results Sixty-eight eligible patients underwent randomisation (34 patients in each group) from April 20, till Jun 20, 2020. In the standard care group, six patients received corticosteroids by the attending physician during treatment and excluded from the ITT population. Patients with clinical improvement were higher in the methylprednisolone group than in the standard care group (94·1% versus 57·1%), and the mortality rate was numerically lower in the methylprednisolone group (5·9% versus 42.9%; p <0·001). We demonstrated that patients in the methylprednisolone intervention group had a significantly increased survival time compared with the patients in the standard care group [Log rank test: p<0.001; Hazard ratio: 0.293; 95% C‎‎I: 0.‎154–0.556]. A total of two patients in each group (5·8% and 7·1% respectively) showed severe adverse events between initiation of treatment and the end of the study.

Conclusions Our results suggested that methylprednisolone pulse could be an efficient therapeutic agent for hospitalised severe COVID-19 patients at the pulmonary phase.

https://erj.ersjournals.com/content/early/2020/09/09/13993003.02808-2020