RecruitingPhase 1Phase 2NCT07629726

A Phase 1/2 Study of KK2430 in Participants With Hematologic Neoplasms

A Phase 1/2, Multicenter, First-in-human Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of KK2430 in Participants With Hematologic Neoplasms


Sponsor

Kyowa Kirin Co., Ltd.

Enrollment

72 participants

Start Date

Aug 1, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

KK2430 ("Study Drug") as a potential treatment for people with Hematologic Neoplasms. KK2430 is an experimental drug; it has not been approved for the treatment of any disease by health authorities such as United States Food and Drug Administration (FDA), and this is the first time it will be given to people. The purpose of this Study is to find out more information about KK2430, whether it is safe in humans, how the body processes it, and if it works for treating your condition.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called KK2430 for people with hematologic neoplasms. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGKK2430

KK2430 administered intravenously


Locations(1)

Prisma Health

Greenville, South Carolina, United States

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NCT07629726


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