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FDA approved Roche’s Actemra for treatment of COVID-19 in hospitalised adults
COVID-19 | FDA | Life Science History

FDA approved Roche’s Actemra for treatment of COVID-19 in hospitalised adults

On Dec. 21, 2022, Roche announced that the U.S. Food and Drug Administration (FDA) had approved Actemraᆴ (tocilizumab)…

Read More FDA approved Roche’s Actemra for treatment of COVID-19 in hospitalised adultsContinue

WHO granted prequalification of Actemra/RoActemra for patients with severe or critical COVID-19
COVID-19 | Life Science History | WHO

WHO granted prequalification of Actemra/RoActemra for patients with severe or critical COVID-19

On Feb. 11, 2022, Roche announced that Actemraᆴ/RoActemraᆴ (tocilizumab) intravenous (IV) had been granted World Health Organization (WHO)…

Read More WHO granted prequalification of Actemra/RoActemra for patients with severe or critical COVID-19Continue

CHMP recommended EU approval of Actemra/RoActemra to treat patients with severe COVID-19
COVID-19 | Life Science History

CHMP recommended EU approval of Actemra/RoActemra to treat patients with severe COVID-19

On Dec. 6, 2021, Roche announced that the European Medicines Agencyメs Committee for Medicinal Products for Human Use…

Read More CHMP recommended EU approval of Actemra/RoActemra to treat patients with severe COVID-19Continue

WHO recommended interleukin-6 receptor blockers for COVID-19 and urged producers to join efforts to rapidly increase access
COVID-19 | Life Science History | WHO

WHO recommended interleukin-6 receptor blockers for COVID-19 and urged producers to join efforts to rapidly increase access

On Jul. 6, 2021, the World Health Organization announced updated patient care guidelines to include interleukin-6 receptor blockers,…

Read More WHO recommended interleukin-6 receptor blockers for COVID-19 and urged producers to join efforts to rapidly increase accessContinue

Humanigen initiated submission for lenzilumab Marketing Authorization in COVID-19, to United Kingdomメs MHRA
Life Science History

Humanigen initiated submission for lenzilumab Marketing Authorization in COVID-19, to United Kingdomメs MHRA

On Jun. 14, 2021 Humanigen announced it had initiated a rolling review submission for Marketing Authorization (MA) by…

Read More Humanigen initiated submission for lenzilumab Marketing Authorization in COVID-19, to United Kingdomメs MHRAContinue

Humanigen reported positive phase 3 results demonstrating Lenzilumabル improved survival without mechanical ventilation with COVID-19
COVID-19 | Life Science History

Humanigen reported positive phase 3 results demonstrating Lenzilumabル improved survival without mechanical ventilation with COVID-19

On Mar. 29, 2021, Humanigen announced positive topline results from its Phase 3 clinical trial evaluating the efficacy…

Read More Humanigen reported positive phase 3 results demonstrating Lenzilumabル improved survival without mechanical ventilation with COVID-19Continue

A common blood test identified which COVID-19 patients benefit and which are harmed from steroid treatment
COVID-19 | Life Science History

A common blood test identified which COVID-19 patients benefit and which are harmed from steroid treatment

On Jul. 22, 2020, a new study led by Albert Einstein College of Medicine and Montefiore Health System…

Read More A common blood test identified which COVID-19 patients benefit and which are harmed from steroid treatmentContinue

Anabolic Steroid Control Act banned OTC steroid precursors and increased penalties for illegal steroids
Biotechnology | Diagnostics | Therapeutics | U.S. Congress

Anabolic Steroid Control Act banned OTC steroid precursors and increased penalties for illegal steroids

In 2004, the U.S. Congress passed the Anabolic Steroid Control Act which enacted a ban on over-the-counter steroid…

Read More Anabolic Steroid Control Act banned OTC steroid precursors and increased penalties for illegal steroidsContinue

Genentech drug Xolair (omalizumab) was approved
Biotechnology | Disease | FDA | Therapeutics

Genentech drug Xolair (omalizumab) was approved

On Jun. 20, 2003, Genentech drug Xolair (omalizumab) was approved by the U. S. Food and Drug Administration…

Read More Genentech drug Xolair (omalizumab) was approvedContinue

Congress passed the Anabolic Steroid Act of 1990, which identified anabolic steroids as a controlled substance
Life Science History | U.S. Congress

Congress passed the Anabolic Steroid Act of 1990, which identified anabolic steroids as a controlled substance

In 1990, responding to increasing illicit traffic, the U.S. Congress passed the Anabolic Steroid Act, which identified anabolic…

Read More Congress passed the Anabolic Steroid Act of 1990, which identified anabolic steroids as a controlled substanceContinue

President Reagan signed the Anti-Drug Abuse Act of 1986, which outlawed the sale of steroids for non-medical purposes
FDA | Medicine | U.S. Congress

President Reagan signed the Anti-Drug Abuse Act of 1986, which outlawed the sale of steroids for non-medical purposes

On Oct. 27, 1986, President Ronald Reagan signed the the Anti-Drug Abuse Act of 1986.  The Act changed…

Read More President Reagan signed the Anti-Drug Abuse Act of 1986, which outlawed the sale of steroids for non-medical purposesContinue

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