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ACTIVE NOT RECRUITING Phase 1

A Study of Oral LOXO-292 (Selpercatinib) in Pediatric Participants With Advanced Solid or Primary Central Nervous System (CNS) Tumors

NCT03899792 · View on ClinicalTrials.gov ↗

Study Summary

This is an open-label, multi-center Phase 1/2 study of oral LOXO-292 in pediatric participants with an activating rearranged during transfection (RET) alteration and an advanced solid or primary CNS tumor.

Interventions

  • DRUG Selpercatinib

Study Locations (20)

Texas

  • University of Texas Southwestern Medical Center at Dallas — Dallas
  • Texas Childrens Hospital — Houston

Other

  • Rigshospitalet — Copenhagen
  • Gustave Roussy — Villejuif

California

  • Childrens Hospital of Los Angeles — Los Angeles

Colorado

  • The Children's Hospital for Cancer and Blood Disorders — Aurora

Florida

  • Nemours Children's Health — Orlando

Massachusetts

  • Dana-Farber Cancer Institute — Boston

Minnesota

  • University of Minnesota Hospital — Minneapolis

New York

  • Memorial Sloan Kettering Cancer Center — New York

Trial Details

FieldValue
Enrollment Target 36 participants
Start Date 2019-06-13
Est. Completion 2029-05
Phase Phase 1

Sponsor

Eli Lilly and Company

704 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03899792

The ClinicalTrials.gov registry entry for NCT03899792 describes a study currently listed as active not 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 36 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Eli Lilly and Company, which has 704 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 5 conditions, with Soft Tissue Sarcoma appearing as the primary indexed condition, and to 1 intervention — of which Selpercatinib 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: NCT03899792 reports 20 study locations spanning 18 distinct geographic areas — top geographies include Texas, Other, California. 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 NCT03899792 about?

NCT03899792 is a clinical study titled "A Study of Oral LOXO-292 (Selpercatinib) in Pediatric Participants With Advanced Solid or Primary Central Nervous System (CNS) Tumors". This is an open-label, multi-center Phase 1/2 study of oral LOXO-292 in pediatric participants with an activating rearranged during transfection (RET) alteration and an advanced solid or primary CNS tumor.

What is the current status of trial NCT03899792?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 36 participants. The study started on 2019-06-13. Estimated completion is 2029-05.

What conditions does trial NCT03899792 study?

This clinical trial studies the following conditions: Soft Tissue Sarcoma, Papillary Thyroid Cancer, Medullary Thyroid Cancer, Infantile Fibrosarcoma, Infantile Myofibromatosis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03899792?

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

Who is sponsoring clinical trial NCT03899792?

This trial is sponsored by Eli Lilly and Company, which has 704 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03899792 being conducted?

This trial has 20 study locations across California, Colorado, Florida, Massachusetts, Minnesota. 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