Recent blog posts
Neurocrine Biosciences Launches Phase 1 Trial to Assess NBI-1076986 in Healthy Participants
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Neurocrine Biosciences Launches Phase 1 Trial to Assess NBI-1076986 in Healthy Participants
11 May 2024
Neurocrine Biosciences, Inc. has launched its Phase 1 clinical trial, marking the first time humans are being evaluated.
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Biotheryx Receives FDA Approval to Begin Trials for BTX-9341, a Novel Dual-Action Degrader Targeting CDK4/6
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Biotheryx Receives FDA Approval to Begin Trials for BTX-9341, a Novel Dual-Action Degrader Targeting CDK4/6
11 May 2024
Biotheryx, Inc. revealed that their Investigational New Drug application for BTX-9341, an innovative bifunctional degrader targeting cyclin-dependent kinase 4/6 (CDK4/6).
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Promising Safety Results from Neurogene's Phase 1/2 Study of NGN-401 Gene Therapy for Rett Syndrome
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Promising Safety Results from Neurogene's Phase 1/2 Study of NGN-401 Gene Therapy for Rett Syndrome
11 May 2024
Neurogene revealed promising safety results from its Phase 1/2 study on NGN-401, a gene therapy for Rett Syndrome.
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FDA Approves Merus' Zeno for Expedited NRG1+ Lung and Pancreatic Cancer Treatment
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FDA Approves Merus' Zeno for Expedited NRG1+ Lung and Pancreatic Cancer Treatment
11 May 2024
Merus Reveals FDA Approval and Expedited Assessment of BLA for Zeno to Manage NRG1+ Lung and Pancreatic Cancer.
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XyloCor Therapeutics Announces Positive Phase 2 Results for XC001 at SCAI 2024, Published in Circulation: Cardiovascular Interventions
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XyloCor Therapeutics Announces Positive Phase 2 Results for XC001 at SCAI 2024, Published in Circulation: Cardiovascular Interventions
10 May 2024
Positive Phase 2 Results for XyloCor Therapeutics’ Main Candidate XC001 Announced at SCAI 2024 and in the Journal Circulation: Cardiovascular Interventions.
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Context Therapeutics Initiates Phase 1 Trial for CTIM-76 Following FDA IND Approval
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Context Therapeutics Initiates Phase 1 Trial for CTIM-76 Following FDA IND Approval
10 May 2024
Context Therapeutics has received FDA approval for its IND application, initiating a Phase 1 clinical trial of CTIM-76.
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Remix Therapeutics Initiates Phase 1 Trials of REM-422 for ACC and AML/MDS Treatment
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Remix Therapeutics Initiates Phase 1 Trials of REM-422 for ACC and AML/MDS Treatment
10 May 2024
Remix Therapeutics has started dosing the first participants in a pair of Phase 1 studies. These trials are testing REM-422 in treating Adenoid Cystic Carcinoma (ACC) and Acute Myeloid Leukemia/Myelodysplastic Syndromes (AML/MDS).
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Alpha-9 Oncology Begins Phase 1 Trial Dosing with A9-3202 in Melanoma Patients
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Alpha-9 Oncology Begins Phase 1 Trial Dosing with A9-3202 in Melanoma Patients
10 May 2024
Alpha-9 Oncology reports initial dosing of the first participant in a phase 1 trial for A9-3202, targeting locally advanced or metastatic melanoma patients.
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Atsena Therapeutics Announces Positive Early Results in Phase 1/2 XLRS Gene Therapy Study
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Atsena Therapeutics Announces Positive Early Results in Phase 1/2 XLRS Gene Therapy Study
10 May 2024
Atsena Therapeutics Reveals Encouraging Results from Initial Group in Phase 1/2 Study of ATSN-201 Gene Treatment for X-linked Retinoschisis (XLRS).
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EyeDNA Therapeutics Presents Promising 2-Year Phase 1/2 Study Results on HORA-PDE6b Therapy for Retinitis Pigmentosa at ARVO
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EyeDNA Therapeutics Presents Promising 2-Year Phase 1/2 Study Results on HORA-PDE6b Therapy for Retinitis Pigmentosa at ARVO
10 May 2024
EyeDNA Therapeutics Reveals Encouraging Two-Year Results at ARVO for its Phase 1/2 Study on HORA-PDE6b Genetic Treatment in Retinitis Pigmentosa Patients with Dual Mutations in PDE6b.
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Adcentrx Therapeutics Gains China's NMPA IND Approval for ADRX-0706, a Nectin-4 Antibody-Drug Conjugate for Advanced Solid Tumors
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Adcentrx Therapeutics Gains China's NMPA IND Approval for ADRX-0706, a Nectin-4 Antibody-Drug Conjugate for Advanced Solid Tumors
10 May 2024
Adcentrx Therapeutics has received IND approval from China's NMPA for ADRX-0706, a new Nectin-4 antibody-drug conjugate designed to treat advanced solid tumors.
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Modalis Therapeutics Reports Promising Outcomes for Novel LAMA2-CMD Treatment, MDL-101
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Modalis Therapeutics Reports Promising Outcomes for Novel LAMA2-CMD Treatment, MDL-101
10 May 2024
Modalis Therapeutics Announces Promising Results for MDL-101, a Novel Epigenome Editing Treatment for LAMA2 Congenital Muscular Dystrophy (LAMA2-CMD).
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