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Beam Therapeutics Announces Clearance of Investigational New Drug Application for BEAM-304 for

Hastings Tribune 18 Jun 2026
BEAM-304 Development Approach Has Potential to Create Transformative, One-time Therapies for the Majority of Patients with PKU ... .
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TuHURA Biosciences Files Investigational New Drug Application for Evaluation of the TBS-2025 VISTA Inhibiting Antibody in Molecularly Defined Subsets of AML and Other Blood Related Cancers

PR Newswire 15 Jun 2026
HURA) ("TuHURA" or the "Company"), a Phase 3 immuno-oncology company developing novel therapeutics to overcome resistance to cancer immunotherapy, today announced that it has filed an Investigational New Drug (IND) application with the U.S.
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TuHURA Biosciences Files Investigational New Drug Application for Evaluation of the TBS-2025 VISTA Inhibiting Antibody in Molecularly Defined Subsets of AML and Other Blood Related Cancers (Tuhura Biosciences Inc)

Public Technologies 15 Jun 2026
... 3 immuno-oncology company developing novel therapeutics to overcome resistance to cancer immunotherapy, today announced that it has filed an Investigational New Drug (IND) application with the U.S.
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Atavistik Bio Announces U.S. FDA Clearance of Investigational New Drug Application and Fast Track Designation ...

Nasdaq Globe Newswire 09 Jun 2026
Atavistik Bio announces U.S. FDA clearance of investigational new drug application and Fast Track Designation for ATV-601 for the treatment of HHT ... .
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Atavistik Bio Announces U.S. FDA Clearance of Investigational New Drug Application and Fast

Hastings Tribune 09 Jun 2026
FDA cleared the Harmony-HHT Phase 1/2 study design, enabling Atavistik Bio to leverage existing clinical data with ATV-1601 and advance directly into a randomized study with individuals who have moderate to severe HHT ... .
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Chengdu Origen and Vanotech Announce KHN921 Investigational New Drug application clearance by the US FDA ...

Nasdaq Globe Newswire 13 May 2026
Investigational New Drug application for KHN921 received “study may proceed” from the US FDA ... Investigational ...
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Cellenkos Announces FDA Clearance of Investigational New Drug (IND) Application for Phase 1b/ 2a Trial of CK0802 in Steroid-Refractory Graft-versus-Host Disease (GVHD)

PR Newswire 04 May 2026
Food and Drug Administration (FDA) has cleared its Investigational New Drug application to initiate a Phase 1b/ 2a clinical trial of CK0802 for the treatment of patients with steroid-refractory graft-versus-host disease (GVHD).
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Cellenkos Announces FDA Clearance of Investigational New Drug (IND) Application for Phase 1b/ 2a Trial ...

Canada Newswire 04 May 2026
Food and Drug Administration (FDA) has cleared its Investigational New Drug application to initiate a Phase 1b/ 2a clinical trial of CK0802 for the treatment of patients with steroid-refractory graft-versus-host disease (GVHD).
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