Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING Phase 1

A Study to Assess a New Medicine Called IPN01195 When Administered Alone in Adults With Advanced Solid Tumours

NCT06833008 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to determine the appropriate dosage, safety and effectiveness of a new study drug IPN01195 in adults with advanced solid tumours. The participants in this study will have advanced solid tumours. 'Advanced solid tumours' refers to cancers that can occur in several places, including cancers in organs or tissues that have spread from their original site to nearby tissues or other parts of the body.

Conditions Studied

Interventions

  • DRUG IPN01195

Study Locations (13)

Other

  • Centre Léon Bérard - Lyon — Lyon
  • Paris Saint-Louis — Paris
  • IGR-Villejuif — Villejuif
  • Istituto Nazionale dei Tumori — Milan
  • Istituto Nazionale Tumori IRCCS - Fondazione Pascale — Naples
  • Val D'Hebron — Barcelona
  • Hospital Universitario Quirónsalud Madrid — Madrid
  • M.D. Anderson Center Madrid — Madrid

Michigan

  • START Mid-West — Grand Rapids

Tennessee

  • Sarah Cannon Research Institute (SCRI) - Nashville — Nashville

Texas

  • Mary Crowley Cancer Research Centers - Medical City Hospital - Dallas — Dallas

Utah

  • START Mountan Region — West Valley City

Virginia

  • Virginia Cancer Specialist- Fairfax — Fairfax

Trial Details

FieldValue
Enrollment Target 85 participants
Start Date 2025-03-14
Est. Completion 2028-10-03
Phase Phase 1

Sponsor

Ipsen

205 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06833008

The ClinicalTrials.gov registry entry for NCT06833008 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 85 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ipsen, which has 205 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Advanced Solid Tumor appearing as the primary indexed condition, and to 1 intervention — of which IPN01195 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: NCT06833008 reports 13 study locations spanning 6 distinct geographic areas — top geographies include Other, Michigan, 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 NCT06833008 about?

NCT06833008 is a clinical study titled "A Study to Assess a New Medicine Called IPN01195 When Administered Alone in Adults With Advanced Solid Tumours". The purpose of this study is to determine the appropriate dosage, safety and effectiveness of a new study drug IPN01195 in adults with advanced solid tumours. The participants in this study will have advanced solid tumours. 'Advanced solid tumours' refers to cancers that can occur in several places...

What is the current status of trial NCT06833008?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 85 participants. The study started on 2025-03-14. Estimated completion is 2028-10-03.

What conditions does trial NCT06833008 study?

This clinical trial studies the following conditions: Advanced Solid Tumor. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06833008?

The interventions under investigation include: IPN01195 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06833008?

This trial is sponsored by Ipsen, which has 205 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06833008 being conducted?

This trial has 13 study locations across Michigan, Tennessee, Texas, Utah, Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial