Recent blog posts
Sirnaomics Announces Successful Phase I clinical trial for STP707, a RNAi therapeutic for addressing multiple solid tumors
Latest Hotspot
4 min read
Sirnaomics Announces Successful Phase I clinical trial for STP707, a RNAi therapeutic for addressing multiple solid tumors
2 September 2023
A striking 74% of assessable patients showcased a premier response of steady disease.
Read →
Initial Dose of ISA104 Administered to First Patient with Chronic Hepatitis B in Phase 1 Human Trials
Latest Hotspot
5 min read
Initial Dose of ISA104 Administered to First Patient with Chronic Hepatitis B in Phase 1 Human Trials
2 September 2023
This inaugural human application (FIH) phase 1 examination, is exploring the efficiency of ISA104
Read →
Alpine Immune Sciences Initiates Administration of 240mg IgA Nephropathy Group in Povetacicept Clinical Trial (RUBY-3)
Latest Hotspot
4 min read
Alpine Immune Sciences Initiates Administration of 240mg IgA Nephropathy Group in Povetacicept Clinical Trial (RUBY-3)
2 September 2023
Alpine Immune Sciences, Inc., has revealed the successful launch of the second IgA nephropathy (IgAN) dosage group in RUBY-3, a phase 1b/2a
Read →
Genexine's long-lasting growth hormone successfully reaches primary endpoint of Phase 3 trial
Latest Hotspot
4 min read
Genexine's long-lasting growth hormone successfully reaches primary endpoint of Phase 3 trial
2 September 2023
Genexine,assessing the efficacy and security of eftansomatropin alfa (an exclusive long-acting growth hormone by Genexine, also referred to as GX-H9) in children suffering from growth hormone deficiency.
Read →
BenevolentAI's Doses First Participants of BEN-8744; Targets PDE10
Latest Hotspot
3 min read
BenevolentAI's Doses First Participants of BEN-8744; Targets PDE10
2 September 2023
BenevolentAI has now informed that its initial subjects have been administered in Phase I first-in-human trials of its oral phosphodiesterase 10 (PDE10) inhibitor, BEN-8744.
Read →
CStone Pharmaceuticals' anti-PD-L1 monoclonal antibody, Sugemalimab, reached its primary endpoint in Phase 3 clinical trials
Latest Hotspot
5 min read
CStone Pharmaceuticals' anti-PD-L1 monoclonal antibody, Sugemalimab, reached its primary endpoint in Phase 3 clinical trials
31 August 2023
Sugemalimab is an anti-PD-L1 monoclonal antibody developed by CStone Pharmaceuticals.
Read →
BridgeBio's TTR stabilizer acoramidis achieves primary endpoint in Phase 3 clinical trial
Latest Hotspot
3 min read
BridgeBio's TTR stabilizer acoramidis achieves primary endpoint in Phase 3 clinical trial
31 August 2023
Recently, BridgeBio Pharma announced that its investigational treatment, acaracides, achieved its primary endpoint in the phase 3 clinical trial.
Read →
Novartis releases positive Phase 3 trial data for its PCSK9-targeted siRNA therapy, inclisiran
Latest Hotspot
4 min read
Novartis releases positive Phase 3 trial data for its PCSK9-targeted siRNA therapy, inclisiran
31 August 2023
On August 29, 2023, Novartis released new long-term data from its ORION-8 Phase 3 clinical trial. The data showed that its twice-yearly RNAi therapy, Leqvio (Inclisiran, Sodium Echociliran), in combination with statins.
Read →
AbbVie's IL-23 antibody Risankizumab completes regulatory filing for new indications in Europe and the United States
Latest Hotspot
3 min read
AbbVie's IL-23 antibody Risankizumab completes regulatory filing for new indications in Europe and the United States
31 August 2023
On August 29, 2023, AbbVie submitted a new indication application to the US FDA and European EMA for Skyrizi (Risankizumab) for the treatment of moderate to severe ulcerative colitis (UC) in adults.
Read →
The European Commission Approves KEYTRUDA® (pembrolizumab) plus Trastuzumab and Chemotherapy, as a treatment for HER2-Positive Advanced Gastric or Gastroesophageal Junction
Latest Hotspot
4 min read
The European Commission Approves KEYTRUDA® (pembrolizumab) plus Trastuzumab and Chemotherapy, as a treatment for HER2-Positive Advanced Gastric or Gastroesophageal Junction
31 August 2023
Merck announced that Merck announced that the European Commission has approved KEYTRUDA, Merck’s anti-PD-1 therapy, in combination with trastuzumab, fluoropyrimidine- and platinum-containing chemotherapy, for the first-line treatment of locally advanced unresectable or metastatic human epidermal growth factor receptor 2 (HER2)-positive gastric or gastroesophageal junction adenocarcinoma in adults whose tumors express PD-L1 (Combined Positive Score≥1).
Read →
AEON Biopharma Discloses Encouraging Outcomes of ABP-450 Phase 2 Clinical Study in Cervical Dystonia
Latest Hotspot
5 min read
AEON Biopharma Discloses Encouraging Outcomes of ABP-450 Phase 2 Clinical Study in Cervical Dystonia
31 August 2023
AEON Biopharma, Inc. has shared encouraging results from their recent Phase 2 medical trial of ABP-450.
Read →
TScan Therapeutics announces their IND application for TSC-203-A0201 received clearance from the FDA
Latest Hotspot
4 min read
TScan Therapeutics announces their IND application for TSC-203-A0201 received clearance from the FDA
31 August 2023
TScan Therapeutics, Inc.announced today that the U.S. FDA has given approval for its new experimental drug TSC-203-A0201, a TCR-T pinpointing PReferentially expressed Antigen in Melanoma.
Read →