Recent blog posts
The initial participant has received a dose in the Phase I clinical study of YOLT-201
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The initial participant has received a dose in the Phase I clinical study of YOLT-201
17 July 2024
YolTech Therapeutics has announced the successful enrollment of the inaugural patient in the Phase I clinical trial of YOLT-201.
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The initial participant enrolled in a Phase 2 trial of Olatec's dapansutrile for Type 2 diabetes patients
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The initial participant enrolled in a Phase 2 trial of Olatec's dapansutrile for Type 2 diabetes patients
17 July 2024
Olatec Therapeutics, Inc., a pioneer in the field of selective NLRP3 inhibitors, revealed that individuals with type 2 diabetes mellitus and associated diabetic complications are currently being recruited
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Vivani Medical Shares New Plans for NPM-115 Small, Long-Term GLP-1 Implant for Obesity
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Vivani Medical Shares New Plans for NPM-115 Small, Long-Term GLP-1 Implant for Obesity
16 July 2024
Vivani Medical, Inc., a pioneering company in biopharmaceuticals, revealed plans to commence the inaugural clinical trial for the NPM-115 initiative in Australia.
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Pfizer Progresses With Daily Dosage Version of Oral GLP-1 Receptor Agonist Danuglipron
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Pfizer Progresses With Daily Dosage Version of Oral GLP-1 Receptor Agonist Danuglipron
16 July 2024
Pfizer have chosen the preferred once-daily modified release form of danuglipron, an oral glucagon-like peptide-1 (GLP-1) receptor agonist.
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Satellos Submits Regulatory Filing to Begin Phase 1 Trial for SAT-3247
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Satellos Submits Regulatory Filing to Begin Phase 1 Trial for SAT-3247
16 July 2024
This submission seeks regulatory approval through the Therapeutic Goods Administration (TGA)’s Clinical Trial Notification scheme to initiate a first-in-human Phase 1 clinical trial for SAT-3247.
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Context Therapeutics Acquires Phase 1-ready T Cell Engager CT-95
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Context Therapeutics Acquires Phase 1-ready T Cell Engager CT-95
16 July 2024
Context Therapeutics Inc. has publicized the acquisition of CT-95, previously the property of Link Immunotherapeutics, Inc.
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Skyhawk Therapeutics Announces Successful Phase 1 Results for SKY-0515 in Huntington's Disease
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Skyhawk Therapeutics Announces Successful Phase 1 Results for SKY-0515 in Huntington's Disease
16 July 2024
Skyhawk Therapeutics Reports Positive Topline Results from Phase 1 Trial of SKY-0515 for Huntington’s Disease, Achieving 72% Reduction in Huntingtin mRNA.
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MEKanistic Therapeutics Inc.'s MTX-531 Shows Tolerability and Tumor Reduction in Preclinical Studies
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MEKanistic Therapeutics Inc.'s MTX-531 Shows Tolerability and Tumor Reduction in Preclinical Studies
16 July 2024
MEKanistic Therapeutics Inc.’s innovative dual-target therapy, MTX-531, shows considerable tolerability and sustained tumor reduction in preclinical cancer studies.
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FDA Approves Rgenta Therapeutics' IND for RGT-61159, an Oral RNA Modulator Targeting ACC and CRC
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FDA Approves Rgenta Therapeutics' IND for RGT-61159, an Oral RNA Modulator Targeting ACC and CRC
15 July 2024
Rgenta Therapeutics secures FDA nod for IND application of RGT-61159, an oral RNA modulator intended to stop MYB production, targeting Adenoid Cystic Carcinoma (ACC) and Colorectal Cancer (CRC).
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Avalo Therapeutics Announces IND Activation for AVTX-009, Targeting Hidradenitis Suppurativa Treatment
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Avalo Therapeutics Announces IND Activation for AVTX-009, Targeting Hidradenitis Suppurativa Treatment
15 July 2024
Avalo Therapeutics Reports IND Activation for AVTX-009, an anti-IL-1β Antibody, Aimed at Treating Hidradenitis Suppurativa.
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uniQure Reports Positive Early Results in AMT-130 Phase I/II Trials for Huntington's Disease
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uniQure Reports Positive Early Results in AMT-130 Phase I/II Trials for Huntington's Disease
15 July 2024
uniQure Releases Promising Interim Results Showing Reduced Disease Progression in Phase I/II AMT-130 Trials for Huntington’s Disease.
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Prelude Therapeutics and Merck to Test PRT3789 with KEYTRUDA® in SMARCA4-Mutated Cancers
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Prelude Therapeutics and Merck to Test PRT3789 with KEYTRUDA® in SMARCA4-Mutated Cancers
15 July 2024
The agreement specifies that the Phase 2 clinical trial will evaluate the effectiveness of PRT37890, a new and highly selective SMARCA2 degrader, and Merck's KEYTRUDA in treating cancers with SMARCA4 mutations.
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