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RSS FeedPosted by Michael Wonder on 27 Jun 2023
FDA accepts Pfizer’s application for haemophilia B gene therapy fidanacogene elaparvovec
27 June 2023 - Submissions based on positive Phase 3 data from BENEGENE-2 trial. ...
Posted by Michael Wonder on 24 Jun 2023
Pfizer and BioNTech submit applications to US FDA for Omicron XBB.1.5 adapted monovalent COVID-19 vaccine
23 June 2023 - The submissions reflect guidance from FDA and other major health authorities to provide COVID-19 vaccines better matched ...
Posted by Michael Wonder on 23 Jun 2023
Moderna files for FDA authorisation of its updated COVID-19 vaccine
22 June 2023 - Preliminary clinical data demonstrated a robust immune response by the company's XBB.1.5 monovalent vaccine against XBB descendent ...
Posted by Michael Wonder on 22 Jun 2023
Aldeyra Therapeutics provides regulatory update on ADX-2191
21 June 2023 - Based on US FDA determination of lack of adequate and well controlled investigations in the scientific literature, ...
Posted by Michael Wonder on 22 Jun 2023
ARS Pharmaceuticals announces PDUFA date extension for neffy (intranasal epinephrine) for the treatment of allergic reactions (type 1), including anaphylaxis
20 June 2023 - Additional time needed for labelling and post-marketing requirements discussions; PDUFA date set for 19 September 2023. ...
Posted by Michael Wonder on 22 Jun 2023
Calliditas Therapeutics submits supplemental new drug application to US FDA for full approval of Tarpeyo
21 June 2023 - Calliditas Therapeutics today announced the submission of a supplemental new drug application to the US FDA ...
Posted by Michael Wonder on 21 Jun 2023
CorMedix announces FDA acceptance of resubmission of new drug application for DefenCath
21 June 2023 - CorMedix today announced that the resubmission of the new drug application for DefenCath has been accepted for ...
Posted by Michael Wonder on 21 Jun 2023
bluebird bio announces FDA priority review of the biologics license application for lovotibeglogene autotemcel (lovo-cel) for patients with sickle cell disease 12 years and older with a history of vaso-occlusive events
21 June 2023 - PDUFA date set for 20 December 2023. ...
Posted by Michael Wonder on 21 Jun 2023
Xbrance announce US FDA filing acceptance for a Lucentis (ranibizumab) biosimilar candidate
21 June 2023 - Xbrane Biopharma today announced the acceptance of the supplemental biologics license application for a Lucentis (ranibizumab) biosimilar ...
Posted by Michael Wonder on 20 Jun 2023
Geron announces submission of new drug application to FDA for first in class telomerase inhibitor imetelstat
20 June 2023 - Geron today announced the submission to the US FDA of a new drug application for imetelstat for ...
Posted by Michael Wonder on 16 Jun 2023
GSK announces extension of FDA review period for momelotinib
16 June 2023 - GSK today announced that the US FDA has extended the review period of the new drug application ...
Posted by Michael Wonder on 15 Jun 2023
FDA accepts for review Medexus's IXinity supplemental biological license application for paediatric patients
15 June 2023 - Expanded indication would cover patients 12 years of age or younger, a population that comprises approximately ...
Posted by Michael Wonder on 15 Jun 2023
Amneal receives NDA approval from FDA for Pemrydi RTU, a ready to use oncology injectable
14 June 2023 - Adds first ready to use presentation of key injectable for treating non-squamous non-small cell lung cancer and ...
Posted by Michael Wonder on 14 Jun 2023
Ipsen announces US FDA submission acceptance of its supplemental new drug application for Onivyde regimen in first-line metastatic pancreatic ductal adenocarcinoma
14 June 2023 - Supplemental new drug application submission based on the NAPOLI 3 Phase 3 trial. ...
Posted by Michael Wonder on 12 Jun 2023
Phathom Pharmaceuticals announces FDA acceptance of NDA resubmission for erosive GERD
12 June 2023 - PDUFA goal date of 17 November 2023. ...