Recent blog posts
HanAll Biopharma Initiates Phase III VELOS-4 Trial of Tanfanercept for Dry Eye Syndrome
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HanAll Biopharma Initiates Phase III VELOS-4 Trial of Tanfanercept for Dry Eye Syndrome
7 May 2024
HanAll Biopharma Launches Phase III Double-Blind, Placebo-Controlled VELOS-4 Study to Assess Tanfanercept in Treating Dry Eye Syndrome.
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TAR-200 Monotherapy Yields High Remission Rates in High-Risk Non-Muscle-Invasive Bladder Cancer
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TAR-200 Monotherapy Yields High Remission Rates in High-Risk Non-Muscle-Invasive Bladder Cancer
7 May 2024
TAR-200 treatment alone achieves over 80% total remission in high-risk patients with non-muscle-invasive bladder cancer.
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Guangzhou Bio-gene Launches Phase I Trial for CLL-1 CAR-T Therapy BG1805
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Guangzhou Bio-gene Launches Phase I Trial for CLL-1 CAR-T Therapy BG1805
7 May 2024
Guangzhou Bio-gene Technologies has launched the first phase of clinical trials for its CAR-T cell therapy BG1805, which targets CLL-1.
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selectION Reveals Encouraging Outcomes from Early-Stage Trial Testing si-544 on Individuals with Eczema
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selectION Reveals Encouraging Outcomes from Early-Stage Trial Testing si-544 on Individuals with Eczema
30 April 2024
selectION, Inc. has shared encouraging outcomes from its initial human Phase 1b study concerning its primary drug, si-544, targeted at individuals with atopic dermatitis.
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AriBio Granted EMA Approval for Phase 3 Trials of AR1001 in Alzheimer’s Treatment (POLARIS-AD)
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AriBio Granted EMA Approval for Phase 3 Trials of AR1001 in Alzheimer’s Treatment (POLARIS-AD)
30 April 2024
AriBio Granted EMA Approval for Phase 3 Trials of AR1001 in Alzheimer’s Treatment (POLARIS-AD).
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FDA Approves Ractigen's RAG-01, a Novel saRNA Therapy for BCG-Resistant NMIBC
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FDA Approves Ractigen's RAG-01, a Novel saRNA Therapy for BCG-Resistant NMIBC
30 April 2024
Ractigen Therapeutics has received FDA clearance for RAG-01, a pioneering saRNA treatment for NMIBC that does not respond to BCG.
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FDA Approves Pfizer's Single-Dose Gene Therapy BEQVEZ™ for Adult Hemophilia B
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FDA Approves Pfizer's Single-Dose Gene Therapy BEQVEZ™ for Adult Hemophilia B
30 April 2024
U.S. FDA Sanctions Single-Dose Gene Treatment BEQVEZ™ (fidanacogene elaparvovec-dzkt) by Pfizer for Adult Hemophilia B Patients.
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Testing Dosage of New T-cell Engager, ARB202, in Advanced Gastrointestinal Cancer Patients
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Testing Dosage of New T-cell Engager, ARB202, in Advanced Gastrointestinal Cancer Patients
30 April 2024
Advanced gastrointestinal cancer patients continue to test dosages with the novel T-cell engager, CDH17 X CD3 cabotamig (ARB202).
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Cidara Therapeutics Retakes Global Rights to CD388, Initiates $240M Funding Drive
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Cidara Therapeutics Retakes Global Rights to CD388, Initiates $240M Funding Drive
28 April 2024
Cidara Therapeutics regains worldwide control for developing and marketing CD388, also launches a $240 million private funding initiative.
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FDA Prioritizes GSK's Proposal to Expand Jemperli Use with Chemotherapy in Advanced Endometrial Cancer
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FDA Prioritizes GSK's Proposal to Expand Jemperli Use with Chemotherapy in Advanced Endometrial Cancer
28 April 2024
FDA has prioritized GSK’s submission to broaden the use of Jemperli (dostarlimab) with chemotherapy for treating all adult patients with initial advanced or relapsed endometrial cancer.
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Alkermes has started the Vibrance-1 Phase 2 trial to assess ALKS 2680 for treating Narcolepsy Type 1
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Alkermes has started the Vibrance-1 Phase 2 trial to assess ALKS 2680 for treating Narcolepsy Type 1
28 April 2024
Alkermes plc has launched the Vibrance-1 study, a phase 2 clinical trial aimed at assessing the safety and effectiveness of ALKS 2680 versus a placebo in individuals diagnosed with type 1 narcolepsy.
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Atom Bioscience begins enrolling U.S. participants in a worldwide Phase 2b/3 study of an experimental chronic gout therapy
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Atom Bioscience begins enrolling U.S. participants in a worldwide Phase 2b/3 study of an experimental chronic gout therapy
28 April 2024
Atom Bioscience focused on innovative therapies for metabolic and inflammatory conditions, has initiated patient enrollment across the United States for a Phase 2b/3 study of ABP-671.
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