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NCT07158918 · ClinicalTrials.gov registry record · Phase 1
ABL103 in Combination With Pembrolizumab, With or Without Taxane in Advanced or Metastatic Solid Tumors
A Phase 1 study of Solid Tumors, sponsored by ABL Bio.
- Recruiting
- Registry status
- Phase 1
- Development phase
- 65
- Enrollment target
- 6
- Study locations
NCT07158918 is a Phase 1 study of Solid Tumors that is actively recruiting participants, run by ABL Bio. The registered enrollment target is 65 participants, below the 284-participant average among 125 other Solid Tumors trials with a reported enrollment target (77% lower). The trial reports 6 study locations across 3 states.
The verdict
NCT07158918, a Phase 1 study of Solid Tumors, is actively recruiting participants, sponsored by ABL Bio.
- RECRUITING
- Registry status
- Phase 1
- Development phase
- 65 participants
- Enrollment target
- 6
- Study locations
Study Summary
This study is to assess the safety and antitumor activity of ABL103 plus pembrolizumab, with or without taxane, in advanced or metastatic solid tumors.
Conditions Studied
Interventions
- DRUG KEYTRUDA® (pembrolizumab)
- DRUG ABL103
- DRUG Taxane
Study Locations (6)
Other
- Seoul National University Bundang Hospital - Seongnam
- Seoul National University Hospital - Seoul
- Asan Medical Center - Seoul
- Samsung Medical Center - Seoul
Ohio
- UH Cleveland Medical Center - Cleveland
Victoria
- PASO Medical - Frankston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 65 participants |
| Start Date | 2025-08-06 |
| Est. Completion | 2027-12-02 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07158918
The ClinicalTrials.gov registry entry for NCT07158918 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 65 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 284-participant average among 125 other Solid Tumors trials with a reported enrollment target (77% lower). The listed sponsor is ABL Bio, which has 3 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Solid Tumors appearing as the primary indexed condition, and to 3 interventions - of which KEYTRUDA® (pembrolizumab) is the first listed.
NCT07158918 reports 6 study locations spanning 3 distinct geographic areas - top geographies include Other, Ohio, Victoria.
Frequently Asked Questions
What is clinical trial NCT07158918 about?
NCT07158918 is a clinical study titled "ABL103 in Combination With Pembrolizumab, With or Without Taxane in Advanced or Metastatic Solid Tumors". This study is to assess the safety and antitumor activity of ABL103 plus pembrolizumab, with or without taxane, in advanced or metastatic solid tumors.
What is the current status of trial NCT07158918?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 65 participants. The study started on 2025-08-06. Estimated completion is 2027-12-02.
What conditions does trial NCT07158918 study?
This clinical trial studies the following conditions: Solid Tumors.
What interventions are being tested in trial NCT07158918?
The interventions under investigation include: KEYTRUDA® (pembrolizumab) (DRUG), ABL103 (DRUG), Taxane (DRUG).
Who is sponsoring clinical trial NCT07158918?
This trial is sponsored by ABL Bio, which has 3 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07158918 being conducted?
This trial has 6 study locations across Ohio, Victoria. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.