US FDA accepts GC Pharma’s biologics license application for immunoglobulin 'GC5107'

5 May 2021 - A significant milestone towards entering the world's largest plasma product marketplace. ...

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Servier announces FDA filing acceptance and priority review for Tibsovo (ivosidenib) in IDH1 mutated cholangiocarcinoma

5 May 2021 - Servier Pharmaceuticals today announced that the U.S. FDA has accepted the company's supplemental new drug application for ...

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Pfizer will file for full FDA approval by end of May

4 May 2021 - Pfizer and BioNTech, the manufacturers of one of the three authorised COVID-19 vaccines in the U.S., plan ...

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ViiV Healthcare initiates rolling submission of new drug application with US FDA for long-acting cabotegravir for prevention of HIV

4 May 2021 - If approved, cabotegravir would be the first, long-acting therapy for HIV PrEP. ...

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SIGA announces new drug application filing with FDA for intravenous formulation of TPOXX

4 May 2021 - Important for patients who cannot swallow oral capsules. ...

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Clearside Biomedical announces resubmission of new drug application for Xipere for treatment of macular oedema associated with uveitis

3 May 2021 - Clearside Biomedical announced today the resubmission of its new drug application to the U.S. FDA for ...

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Intra-Cellular Therapies announces FDA acceptance of Caplyta (lumateperone) sNDAs for the treatment of bipolar depression

3 May 2021 - Intra-Cellular Therapies today announced that the U.S. FDA has accepted for review its supplemental new drug applications ...

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Hutchmed completes rolling submission of NDA to U.S. FDA for surufatinib for the treatment of advanced neuroendocrine tumours

3 May 2021 - First NDA submission by Hutchmed in the U.S.; product launch preparations underway. ...

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U.S. Food and Drug Administration accepts for priority review Bristol Myers Squibb’s application for Opdivo (nivolumab) as adjuvant treatment for patients with muscle-invasive urothelial carcinoma

30 April 2021 - Application based on Phase 3 CheckMate-274 trial, in which Opdivo nearly doubled disease-free survival compared to placebo. ...

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Update on U.S. FDA review of LEO Pharma’s biologics license application for tralokinumab for the treatment of adults with moderate to severe atopic dermatitis

29 April 2021 - FDA has requested additional data relating to a device component of tralokinumab. ...

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Biogen provides regulatory update on the supplemental biologic license application for subcutaneous administration of Tysabri (natalizumab)

28 April 2021 - Biogen today announced that it has received a complete response letter from the U.S. FDA for ...

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FDA grants priority review for Nefecon for patients with IgA nephropathy

28 April 2021 - Calliditas Therapeutics today announced that the U.S. FDA has accepted the submission and granted priority review for ...

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FDA begins review of GC Pharma’s blood product for marketing authorisation

27 April 2021 - The U.S. FDA has entered a full review of GC Pharma’s intravenous immunoglobulin therapy GC5107 for ...

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Takeda announces U.S. FDA grants priority review for new drug application for mobocertinib (TAK-788) as a treatment for EGFR exon 20 insertion positive metastatic non-small cell lung cancer

28 April 2021 - Prescription Drug User Fee Act target action date set for 26 October 2021. ...

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Sol-Gel Technologies provides update on FDA review of Epsolay

27 April 2021 - Sol-Gel Technologies today announced an update regarding the U.S. FDA approval process for Epsolay (benzoyl peroxide) ...

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