Vanda Pharmaceuticals announces FDA update for supplemental NDA for Hetlioz in the treatment of insomnia

6 March 2024 - Vanda Pharmaceuticals today announced that on 4 March 2024, it received a complete response letter from ...

Read more →

Camurus announces FDA acceptance of NDA submission for Oclaiz for treatment of acromegaly

5 March 2024 - PDUFA set to 21 October 2024. ...

Read more →

Zevra Therapeutics provides FDA update on the PDUFA action date for arimoclomol as a treatment for Niemann-Pick disease type C

4 March 2024 - The new PDUFA action date set by the FDA is 21 September 2024. ...

Read more →

SpringWorks Therapeutics initiates rolling submission of new drug application to the FDA for mirdametinib for the treatment of children and adults with NF1-PN

4 March 2024 - SpringWorks Therapeutics announced today that the Company has initiated a rolling submission of a new drug application ...

Read more →

Intercept announces FDA acceptance of supplemental new drug application for Ocaliva (obeticholic acid) for the treatment of PBC

29 February 2024 - FDA has assigned a PDUFA target action date of 15 October 2024. ...

Read more →

Applied Therapeutics announces FDA acceptance and priority review of new drug application for govorestat for the treatment of classic galactosaemia

28 February 2024 - PDUFA target action date of 28 August 2024. ...

Read more →

Incyte announces US FDA grants priority review for axatilimab for the treatment of chronic graft versus host disease

27 February 2024 - Priority review acceptance based on positive results of AGAVE-201 study. ...

Read more →

Theratechnologies receives refusal to file letter for Trogarzo intramuscular method of administration sBLA from FDA

27 February 2024 - Theratechnologies today announced that the US FDA has issued a refusal to file letter regarding the Company’s ...

Read more →

BeiGene’s biologics license application for Tevimbra (tislelizumab) for first-line gastric or gastro-oesophageal junction cancers accepted by FDA

27 February 2024 - Application based on results from global Phase 3 RATIONALE-305 trial demonstrating Tevimbra plus chemotherapy significantly improved overall ...

Read more →

Minerva Neurosciences receives complete response letter from FDA for new drug application for roluperidone for the treatment of negative symptoms in patients with schizophrenia

27 February 2024 - Minerva Neurosciences announced today that the US FDA has issued a complete response letter to the ...

Read more →

US FDA accepts for priority review the supplemental biologics license application for epcoritamab (Epkinly) for difficult to treat relapsed or refractory follicular lymphoma

26 February 2024 - FDA grants priority review with target action date of 28 June 2024. ...

Read more →

Dupixent (dupilumab) sBLA accepted for FDA priority review for treatment of COPD with type 2 inflammation

23 February 2024 - Priority review granted based on positive results from two Phase 3 trials; if approved, Dupixent would be ...

Read more →

US FDA grants priority review to Harmony Biosciences' application for Wakix (pitolisant) in paediatric narcolepsy

21 February 2024 - Prescription Drug User Fee Act date is 21 June 2024. ...

Read more →

Linvoseltamab BLA for treatment of relapsed/refractory multiple myeloma accepted for FDA priority review

21 February 2024 - Regeneron Pharmaceuticals today announced that the US FDA has accepted for priority review the biologics license application ...

Read more →

FDA and EMA accept vorasidenib regulatory submissions for the treatment of IDH mutant diffuse glioma

20 February 2024 - In clinical studies, vorasidenib has demonstrated strong blood-brain barrier penetrance alongside clinically meaningful and statistically significant ...

Read more →