Ozmosi | Potrasertib Drug Profile
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Potrasertib

Alternative Names: Potrasertib, imp-7068, imp7068, imp 7068
Clinical Status: Active
Latest Update: 2023-06-01
Latest Update Note: News Article

Product Description

IMP7068 is a potent and selective WEE1 inhibitor. The preliminary result of the safety, tolerability, pharmacokinetic, pharmacodynamic profiles and antitumor activity of IMP7068 in patients with advanced solid tumors in the monotherapy dose escalation part of the study was presented. Thirty-two patients were enrolled in eight dose cohorts. Median follow-up duration was 212 days, and one patient (uterine serous carcinoma) had a best overall response of partial response. The rate of treatment-related adverse event (TRAE) was 65.6%, and TRAEs were mostly grade 1–2. IMP7068 was well-tolerated, and its PK and PD profiles were consistent with WEE1 inhibition and were dose dependent. (Sourced from: http://www.impacttherapeutics.com/en/new/162.html)

Mechanisms of Action: WEE1 Inhibitor

Novel Mechanism: Yes

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Impact Therapeutics
Company Location:
Company CEO:
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Potrasertib

Countries in Clinic: China, Taiwan, United States

Active Clinical Trial Count: 1

Recent & Upcoming Milestones

Highest Development Phases

Phase 1: Oncology Solid Tumor Unspecified

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

CTR20212068

P1

Recruiting

Oncology Solid Tumor Unspecified

None

2025-04-29

Patient Enrollment|Start Date|Treatments|Trial Status