Ozmosi | Pamlectabart tismanitin Drug Profile
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Pamlectabart tismanitin

Pronounced as: pam-LEK-ta-bart tis-MAN-i-tin

Alternative Names: Pamlectabart tismanitin, hdp-101, hdp101, hdp 101
Clinical Status: Active
Latest Update: 2025-06-06
Latest Update Note: News Article

Product Description

HDP-101, an Anti-BCMA Antibody-Drug Conjugate, Safely Delivers Amanitin to Induce Cell Death in Proliferating and Resting Multiple Myeloma Cells. (Sourced from: https://pubmed.ncbi.nlm.nih.gov/33298585/)

Mechanisms of Action: BCMA Inhibitor

Novel Mechanism: No

Modality: Antibody Drug Conjugate

Route of Administration: Intravenous

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Huadong Pharmaceutical Group New Drug Research Institute
Company Location: Asia Pacific
Company Founding Year: 1993
Additional Commercial Interests: Heidelberg Pharma

Clinical Description

Map of Global Clinical Trials for Pamlectabart tismanitin

Countries in Clinic: Germany, Hungary, Poland, United States

Active Clinical Trial Count: 2

Recent & Upcoming Milestones

Highest Development Phases

Phase 2: Multiple Myeloma|Paraproteinemias

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

2024-515273-10-00

HDP-101-01

P2

Recruiting

Multiple Myeloma

2026-05-26

2025-05-02

Treatments

NCT04879043

HDP-101-01

P2

Recruiting

Paraproteinemias|Multiple Myeloma

2025-08-01

33%

2024-07-25

Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments