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A Study to Evaluate INCA036873 in Participants With Advanced Solid Tumors and Hematological Malignancies
NCT07195916 · View on ClinicalTrials.gov ↗
Study Summary
A study to evaluate the safety and tolerability of INCA036873 in participants with advanced solid tumors and hematological malignancies.
Conditions Studied
Interventions
- DRUG INCA036873
Study Locations (20)
Other
- Cliniques Universitaires Ucl Saint-Luc — Brussels
- Universitair Ziekenhuis Antwerpen — Edegem
- Universitair Ziekenhuis Gent (Uz Gent) — Ghent
- Universitair Ziekenhuis Leuven — Leuven
- Aarhus University Hospital — Aarhus
- Rigshospitalet Uni of Hospital of Copenhagen — Copenhagen
- Aou Policlinico S. Orsola-Malpighi — Bologna
- Fondazione Irccs Istituto Nazionale Dei Tumori — Milan
California
- City of Hope Medical Center — Duarte
- University of California San Diego Medical Center, Moores Cancer Center — La Jolla
Tennessee
- Scri Oncology Partners — Nashville
- Vanderbilt Medical Center — Nashville
Michigan
- University of Michigan — Ann Arbor
Nebraska
- The University of Nebraska Medical Center — Omaha
New York
- Memorial Sloan Kettering Cancer Center — New York
Texas
- Md Anderson Cancer Center — Houston
New South Wales
- Macquarie University Hospital — Sydney
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 280 participants |
| Start Date | 2026-01-08 |
| Est. Completion | 2028-08-18 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07195916
The ClinicalTrials.gov registry entry for NCT07195916 describes a study currently listed as recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 280 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Incyte Corporation, which has 163 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Solid Tumors appearing as the primary indexed condition, and to 1 intervention — of which INCA036873 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT07195916 reports 20 study locations spanning 11 distinct geographic areas — top geographies include Other, California, Tennessee. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT07195916 about?
NCT07195916 is a clinical study titled "A Study to Evaluate INCA036873 in Participants With Advanced Solid Tumors and Hematological Malignancies". A study to evaluate the safety and tolerability of INCA036873 in participants with advanced solid tumors and hematological malignancies.
What is the current status of trial NCT07195916?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 280 participants. The study started on 2026-01-08. Estimated completion is 2028-08-18.
What conditions does trial NCT07195916 study?
This clinical trial studies the following conditions: Solid Tumors, Hematologic Malignancies. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT07195916?
The interventions under investigation include: INCA036873 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT07195916?
This trial is sponsored by Incyte Corporation, which has 163 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT07195916 being conducted?
This trial has 20 study locations across California, Michigan, Nebraska, New York, Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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