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BioWorld - Thursday, June 25, 2026
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Regulatory actions for March 7, 2022

March 7, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Amgen, Aravax, Bharat Biotech, Biogen, Eisai, Merck, Nymox, Ocugen.
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In the clinic for March 7, 2022

March 7, 2022

Clinical updates, including trial initiations, enrollment status and data readouts and publications: American Cryostem, Aravive, Atreca, Coherus, Eli Lilly, Equillium, Evofem, Incyte, Mink, Recursion.


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Regulatory actions for March 4, 2022

March 4, 2022
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Circa Scientific, KSL Diagnostics, SQI Diagnostics.
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Person using COVID-19 antigen test at home

FDA clamping down on rapid antigen tests for COVID-19

March 3, 2022
By Mark McCarty
The FDA continues its tight surveillance of rapid antigen tests for the COVID-19 pandemic and has issued three safety communications advising against the use of these tests thus far in the month of March. In each instance, the test is made by the manufacturer of name, but was not authorized in the U.S., making these misbranded products despite their legal use in other nations.
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Clinical data illustration

With fewer pandemic updates, clinical data down by 11%

March 3, 2022
By Karen Carey
While clinical trial updates in 2022 started off slow, the gap with last year appears to be closing, even as pandemic activity diminishes.
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Pause in recruitment to REMAP CAP COVID-19 trial affects Dimerix’s lead candidate, DMX-200

March 3, 2022
By Tamra Sami
PERTH, Australia – The independent data safety monitoring board of the global REMAP-CAP COVID-19 study has uncovered a concerning safety signal in treatment arms that include an angiotensin converting enzyme inhibitor and an angiotensin receptor blocker in patients with severe COVID-19, and it has recommended that recruitment be suspended for those treatment arms.
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Elderly patient in hospital bed

Olumiant reduces risk of COVID-19 death, as Recovery trial continues

March 3, 2022
By Nuala Moran
LONDON – The U.K. Recovery trial has added a fourth drug to the list of therapies it has shown are effective in treating hospitalized COVID-19 patients, demonstrating the JAK inhibitor Olumiant (baricitinib) reduces the risk of death by 13% in seriously ill patients. That effect is in addition to treatment with dexamethasone, which became standard of care after the Recovery trial showed it reduced mortality by one-third in patients on ventilators.
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Other news to note for March 3, 2022

March 3, 2022
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: A2, Aquestive, Athira, Autolus, Avenge, Haisco, Inspirevax, Oragenics, Sorrento, Spexis.
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Regulatory actions for March 2, 2022

March 2, 2022
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Dexcom, Gleamer, Intrivo, J&J Vision, Valencia Technologies.
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Health Canada office sign

Canada’s COVID-19 interim orders giving way to regulations

March 2, 2022
By Mari Serebrov
New drug and device regulations going into effect in Canada are serving as a reminder of the extended life of the COVID-19 pandemic. After two years of interim orders regulating the importation and sale of drugs and devices for COVID-19 clinical trials and the conduct of those trials, Canada is issuing long-term regulations that will incorporate most of the provisions of the temporary orders.
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