CI

At a glance

ClinicalIndex Comparison Record
Early Ph 1Recruiting· 150 target
Drug / intervention
SPH5030 tabletsdrug
Likely dose
Not stated in 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/NCT05245058
NCT05245058Early Ph 1RecruitingOn Track
Long Recruiting

A Phase I Study to Evaluate the Safety, Tolerability, and Pharmacokinetic Characteristics of SPH5030 Tablets in Subjects With Advanced Her2-positive Solid Tumors

Shanghai Pharmaceuticals Holding Co., Ltd·interventional·Posted Feb 17, 2022·Updated May 5, 2026

In Brief

A Early Phase 1 clinical trial evaluating SPH5030 tablets for HER2-positive Advanced Solid Tumors. Currently recruiting, targeting 150 participants across 17 sites.

Detailed Summary

To evaluate the safety and tolerability of SPH5030 tablets in subjects with HER2-positive advanced solid tumors

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

Early Ph 1Recruiting
202220232024202520262027
First PostedFeb 17, 2022
Enrollment StartJan 21, 2022
Primary CompletionDec 21, 2026
TodayJul 1, 2026
Enrollment to primary: 4.9 yearsPosted 4.4 years agoPrimary completion in 6 months

Interventions

SPH5030 tabletsdrug

SPH5030 tablets orally once or twice daily.