CI

At a glance

ClinicalIndex Comparison Record
Phase 2Recruiting· 50 target
Drug / intervention
Avatrombopagdrug
Likely dose
Avatrombopag 60 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05218226
NCT05218226Phase 2RecruitingUpdate OverdueUpdated 16mo ago · Completion was 17mo ago
Enrollment Stalled
Long Recruiting
Update Overdue

Avatrombopag for Chemotherapy-induced Thrombocytopenia in Solid Tumors: a Prospective Multi-center One-arm Study

Institute of Hematology & Blood Diseases Hospital, China·interventional·Posted Feb 1, 2022·Updated Feb 24, 2025

In Brief

A Phase 2 clinical trial evaluating Avatrombopag for Chemotherapy-induced Thrombocytopenia and Avatrombopag. Currently recruiting, targeting 50 participants across 1 site.

Signals

Enrollment appears stalled

Detailed Summary

To evaluate the efficacy and safety of Avatrombopag to treat chemotherapy-induced thrombocytopenia in solid tumors

Study Details

Timeline

Phase 2RecruitingOverdue
20222023202420252026
First PostedFeb 1, 2022
Enrollment StartFeb 10, 2022
Primary CompletionDec 31, 2024
Study CompletionDec 31, 2025
TodayJul 1, 2026
Enrollment to primary: 2.9 yearsPosted 4.4 years ago

Interventions

Avatrombopagdrug

The subjects will initiate treatment with 60 mg/d Avatrombopag. Platelet counts is obtained weekly and dose adjustment should be done according to platelet counts, and maximum dose should not exceed 60 mg daily. Subjects whose platelet count ≤100×109/L,the Avatrombopag dose will maintain. If platelet count \>100×109/L for 2 weeks, the subjects need to reduce the dose of Avatrombopag to the next lower dose or lower frequency. If subjects whose platelet count exceeds 100×109/L for 4 weeks,already have reduced the dose of Avatrombopag to 20mg once every other day or lower frequency during the treatment period, Avatrombopag can be stopped for observation, until platelet counts fall below 100×109/L. If the subjects do not need further chemotherapy or radiotherapy, the subjects can taper off Avatrombopag if the platelet is greater than 50×109/L.