Recent blog posts
Initial Trial of CytomX's CX-2051, a Targeted ADC for Solid Tumors
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Initial Trial of CytomX's CX-2051, a Targeted ADC for Solid Tumors
12 April 2024
CytomX Therapeutics has revealed initial treatment using CX-2051, a selective EpCAM-targeted antibody-drug conjugate, in an early-stage trial involving individuals with progressive solid malignancies.
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CHS-1000 - A Novel ILT4 Antagonist Unveiled at AACR 2024
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CHS-1000 - A Novel ILT4 Antagonist Unveiled at AACR 2024
12 April 2024
CHS-1000, an Innovative ILT4 Antagonist Antibody, Showcased Through Early-Stage Research at AACR's 2024 Gathering.
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Vivet Therapeutics Begins Phase 1/2 Trial Dosage for Second Group in Wilson Disease Study
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Vivet Therapeutics Begins Phase 1/2 Trial Dosage for Second Group in Wilson Disease Study
11 April 2024
Vivet Therapeutics Administers Initial Dose to First Participant in Second Group of Phase 1/2 GATEWAY Study for Wilson Disease Therapy.
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Clover Reveals Encouraging Early Data for SCB-1019, a Dual RSV Immunization, in First Group of Young Adults
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Clover Reveals Encouraging Early Data for SCB-1019, a Dual RSV Immunization, in First Group of Young Adults
11 April 2024
Promising Early Results for SCB-1019 Vaccine in Young Adults: Clover Biopharmaceuticals Phase I Insights.
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Glenmark Ichnos Sciences Exhibits Early-Stage Results of Cancer Drug Candidate ISB 2001 at 2024 AACR Conference
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Glenmark Ichnos Sciences Exhibits Early-Stage Results of Cancer Drug Candidate ISB 2001 at 2024 AACR Conference
11 April 2024
Ichnos Glenmark Innovation Unveils Early Findings for Cancer Candidate ISB 2001 at AACR 2024.
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Mabwell's Subsidiary T-mab Gets Approval for Denosumab Injection from National Medical Agency
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Mabwell's Subsidiary T-mab Gets Approval for Denosumab Injection from National Medical Agency
11 April 2024
Mabwell has declared that its fully-owned subsidiary, T-mab, has successfully received the green light for its Denosumab Injection from the National Medical Products Administration.
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HLX14 Biosimilar Meets Goals in Phase 3 Trial Against Prolia® and Xgeva®
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HLX14 Biosimilar Meets Goals in Phase 3 Trial Against Prolia® and Xgeva®
11 April 2024
Primary Objectives Achieved in Stage 3 Trial for HLX14, a Biosimilar Contender to Prolia® and Xgeva® (denosumab).
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Ferring Presents Phase 3 Findings for SI-6603 in Back Disc Protrusion at ASIPP 2024
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Ferring Presents Phase 3 Findings for SI-6603 in Back Disc Protrusion at ASIPP 2024
11 April 2024
Ferring Unveils Key Phase 3 Results for Experimental Therapy, SI-6603 (condoliase), in Treating Lower Back Disc Protrusion during ASIPP 2024.
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U.S. Approves ENHERTU® for HER2 Positive Metastatic Solid Cancers Post-Initial Treatment
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U.S. Approves ENHERTU® for HER2 Positive Metastatic Solid Cancers Post-Initial Treatment
9 April 2024
U.S. Sanctions ENHERTU®, a Pioneer HER2-Targeting Drug, for Metastatic Solid Cancers with HER2 Positivity After Initial Treatments.
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FDA Approves Abecma for Hard-to-Treat Multiple Myeloma Post-Two Therapies
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FDA Approves Abecma for Hard-to-Treat Multiple Myeloma Post-Two Therapies
9 April 2024
FDA Clears Abecma from Bristol Myers and 2seventy bio for Treatment of Relapsed or Stubborn Multiple Myeloma Following Two Previous Therapies.
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Immunome to Showcase Early Research on Its Primary Radiotherapy Agent, IM-3050, at the AACR Meeting in 2024
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Immunome to Showcase Early Research on Its Primary Radiotherapy Agent, IM-3050, at the AACR Meeting in 2024
9 April 2024
Immunome, Inc. plans to reveal early data on IM-3050, their lead drug featuring lutetium-177, targeting the fibroblast activation protein.
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Werewolf Therapeutics Unveils Promising Results of WTX-518 and WTX-712 in Cancer Treatment Trial
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Werewolf Therapeutics Unveils Promising Results of WTX-518 and WTX-712 in Cancer Treatment Trial
9 April 2024
Werewolf Therapeutics Reveals Early Stage Study Outcomes Highlighting the Cancer-Fighting Capabilities of Immune-Stimulating Drugs WTX-518 and WTX-712.
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