Biotechnology company Armata Pharmaceuticals Inc (NYSE American: ARMP) reported on Monday that it has received U.S. Food and Drug Administration Breakthrough Therapy designation for AP-SA02, its intravenous multi-phage product candidate for adjunct treatment of complicated Staphylococcus aureus bacteremia caused by MSSA or MRSA.
The designation is supported by Phase 1b/2a diSArm study data showing AP-SA02 plus best available antibiotic therapy was well tolerated and produced higher and earlier clinical cure rates than placebo plus antibiotics. At 28 days after completion of antibiotic treatment, 100% of AP-SA02-treated patients maintained a clinical response without relapse, compared with 75% for placebo.
AP-SA02 already holds FDA Fast Track and Qualified Infectious Disease Product designations. Armata plans to advance the candidate into a Phase 3 superiority study in complicated bacteremia, expected to begin in the second half of 2026.
Seismic Pharmaceuticals enrols first patient in istaroxime global Phase 3 trial in cardiogenic shock
BioEdge Research Labs advances transparency in research compound documentation
Insilico Medicine doses first patient in Phase III trial of rentosertib
BridgeBio reports exploratory PROPEL 3 data showing wider clinical trends for oral infigratinib
Tyra Biosciences declares positive Phase 2 results for oral dabogratinib in bladder cancer
Harbour BioMed partner raises USD225m to advance neoadjuvant immuno-oncology therapy porustobart
Kazia Therapeutics doses first patient in paediatric AT/RT study
Fusion Antibodies secures Canadian patent for OptiMAL
Revvity to acquire Human Cell Design to expand metabolic disease drug discovery capabilities
Biophytis expands BIO101 obesity study to assess weight regain
THX Pharma secures European patent for Batten-1 in juvenile Batten disease
Orphalan commences Phase 3 study of trientine therapy in Wilson disease
ZAGENO named Frost & Sullivan's 2026 North American Life Sciences E-Commerce Company of the Year
Pharvaris reports Phase 3 success for deucrictibant XR in HAE prophylaxis