Drugs / KT501
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KT501

Monoclonal antibody targets CD19 via depletion

Developed for
rheumatoid arthritis
Investigated by
Kali Therapeutics, Inc.

Trials 1

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1 NCT07234773 Mar 2026 → Feb 2027 expected rheumatoid arthritis Kali Therapeutics, Inc. Recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 1

DateIssuerRelease
2026-09-03 Kali Therapeutics, Inc. Regulatory Kali Therapeutics Receives U.S. FDA Clearance for KT501 InvestigationalNew Drug Application kalitherapeutics.com ↗
Kali Therapeutics, a clinical-stage biotechnology company pioneering next-generation immune-resetting and multi-specific therapies, today announced that the U.S. Food and Drug Administration (FDA) has cleared the company’s Investigational New Drug (IND) application for KT501.

Evidence & citations 5 cited values

Every value below carries the sentence it was read from. 1 source stands behind the page.

FieldValueCited text
Known as KT501 ClinicalTrials.gov intervention name — accepted as the source's own label NCT07234773 ↗
Action Deplete “depletes B cells including plasma cells” NCT07234773 ↗
Modality Monoclonal antibody “KT501 is a monoclonal antibody” NCT07234773 ↗
Route Subcutaneous “administered subcutaneously” NCT07234773 ↗
Target CD19 “targeting CD19, BCMA and CD3” NCT07234773 ↗