Ozmosi | YKST-02 Drug Profile
Drug Profile
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YKST-02

Alternative Names: YKST-02, YKST 02, YKST02
Clinical Status: Active
Latest Update: 2026-07-10
Latest Update Note: Clinical Trial Update

Product Description

YKST02, developed by Excyte, is a bispecific antibody with a 2+2 symmetric structure based on the company's unique fusion of IgG and scFv technology (FIST) platform. It is positioned to be a best-in-class drug for multiple myeloma patients, utilizing the same mechanism of action as BCMA-targeting CAR-T therapy. Preclinical data shows that YKST02 is safer and more effective than Teclistamab from J&J. The Investigational new drug (IND) application was submitted to the Center for drug evaluation (CDE) of National Medical Product Administration (NMPA) China on February 26, 2024, and approved within two months, demonstrating the sufficiency of the preclinical study data for clinical trials. It is an anti-CD3×BCMA. (Sourced from: http://www.iexcyte.com/news/shownews.php?id=189&lang=en)

Mechanisms of Action: BCMA Inhibitor, CD3 Inhibitor

Novel Mechanism: No

Modality: Bispecific Antibody

Route of Administration: Intravenous

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Company: Excyte Biopharma Ltd
Company Location:
Company Founding Year: None
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for YKST-02

Countries in Clinic: China

Active Clinical Trial Count: 3

Recent & Upcoming Milestones

Highest Development Phases

Phase 2: Multiple Myeloma

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT06574568

YKST02-I-01

P1

Recruiting

Multiple Myeloma

2026-12-31

50%

2024-09-20

Primary Endpoints|Treatments

CTR20241570

CTR20241570

P1

Recruiting

Multiple Myeloma

None

2025-04-29

Patient Enrollment|Start Date|Treatments|Trial Status

NCT07695740

YKST02-Ⅱ-01

P2

Not yet recruiting

Multiple Myeloma

2029-09-01

50%

2026-07-11

Primary Endpoints|Treatments

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