Recent blog posts
SanBio's AKUUGO® for Treating Motor Paralysis in Brain Injury Patients: Approval Achieved
Latest Hotspot
3 min read
SanBio's AKUUGO® for Treating Motor Paralysis in Brain Injury Patients: Approval Achieved
6 August 2024
SanBio Gains Approval for "AKUUGO® Suspension for Intracranial Use" (INN: Vandefitemcel) to Treat Persistent Motor Paralysis from Traumatic Brain Injuries.
Read →
BioNTech Reports Positive Phase 2 Outcomes for mRNA Therapy BNT111 in Advanced Melanoma Patients
Latest Hotspot
3 min read
BioNTech Reports Positive Phase 2 Outcomes for mRNA Therapy BNT111 in Advanced Melanoma Patients
5 August 2024
The combination therapy was well tolerated, and the safety profile of BNT111 with cemiplimab was consistent with previous trials of BNT111 with anti-PD-(L)1-based treatments.
Read →
Tectonic Therapeutic Secures US IND Approval for TX45 Lead Program
Latest Hotspot
3 min read
Tectonic Therapeutic Secures US IND Approval for TX45 Lead Program
5 August 2024
Tectonic Therapeutic has announced that the U.S. Food and Drug Administration has approved its Investigational New Drug application for TX45.
Read →
Pamrevlumab Trial Results in Advanced Pancreatic Cancer: FibroGen's Update
Latest Hotspot
3 min read
Pamrevlumab Trial Results in Advanced Pancreatic Cancer: FibroGen's Update
5 August 2024
FibroGen Releases Main Outcomes from Two Advanced Pamrevlumab Pancreatic Cancer Trials and Shares Corporate News.
Read →
FDA Clears IND for Umoja's UB-VV111: A CD19 CAR T-Cell Therapy for Blood Cancers
Latest Hotspot
3 min read
FDA Clears IND for Umoja's UB-VV111: A CD19 CAR T-Cell Therapy for Blood Cancers
5 August 2024
Umoja Biopharma Receives FDA Approval for IND Application of UB-VV111, a CD19 Targeted CAR T for Blood Cancers.
Read →
EMA Approves Bio-Thera's BAT1706: A Bevacizumab Biosimilar to Avastin®
Latest Hotspot
2 min read
EMA Approves Bio-Thera's BAT1706: A Bevacizumab Biosimilar to Avastin®
5 August 2024
The European Medicines Agency (EMA) has given its approval to Bio-Thera Solutions for BAT1706 (Avzivi®, bevacizumab), a biosimilar of Avastin®.
Read →
Connext Successfully Gives Initial CNT201 Dose for Dupuytren’s Contracture
Latest Hotspot
3 min read
Connext Successfully Gives Initial CNT201 Dose for Dupuytren’s Contracture
5 August 2024
Connext has revealed the initial successful administration of CNT201, its therapeutic solution for Dupuytren’s contracture, in patients.
Read →
FDA Approves Vertex's Suzetrigine for Moderate-to-Severe Acute Pain
Latest Hotspot
3 min read
FDA Approves Vertex's Suzetrigine for Moderate-to-Severe Acute Pain
2 August 2024
Vertex reveals FDA approval of New Drug Application for Suzetrigine for treating moderate-to-severe acute pain.
Read →
PepGen Announces Promising Low-Dose Results in Phase 2 CONNECT1-EDO51 Trial for Duchenne Muscular Dystrophy Treatment
Latest Hotspot
3 min read
PepGen Announces Promising Low-Dose Results in Phase 2 CONNECT1-EDO51 Trial for Duchenne Muscular Dystrophy Treatment
2 August 2024
PepGen reports encouraging results from low-dose group in ongoing CONNECT1-EDO51 Phase 2 trial for treating Duchenne Muscular Dystrophy with PGN-EDO51.
Read →
Formycon initiates Phase III clinical trial for Keytruda® biosimilar candidate FYB206
Latest Hotspot
3 min read
Formycon initiates Phase III clinical trial for Keytruda® biosimilar candidate FYB206
2 August 2024
Formycon AG announced the first enrollment in the Phase III "Lotus" study comparing FYB206/pembrolizumab with leading cancer drug Keytruda for safety and efficacy.
Read →
Celldex Reports Successful Phase 2 Results for Barzolvolimab in Chronic Inducible Urticaria
Latest Hotspot
2 min read
Celldex Reports Successful Phase 2 Results for Barzolvolimab in Chronic Inducible Urticaria
2 August 2024
Celldex Therapeutics announces successful findings from Phase 2 trial of Barzolvolimab for chronic inducible urticaria.
Read →
undefined European Commission gives green light to Roche's Vabysmo for treating retinal vein occlusion (RVO)
Latest Hotspot
3 min read
undefined European Commission gives green light to Roche's Vabysmo for treating retinal vein occlusion (RVO)
2 August 2024
Roche disclosed today that the European Commission has given the green light to Vabysmo® (faricimab) .
Read →