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

COMPLETED Phase 1

LYT-200 Alone and in Combination With Chemotherapy or Tislelizumab in Patients With Locally Advanced or Metastatic Solid Tumors

NCT04666688 · View on ClinicalTrials.gov ↗

Study Summary

A Phase 1/2 Open-label, Multi-center Study of the Safety, Pharmacokinetics, and Anti-tumor Activity of LYT-200 Alone and in Combination with Chemotherapy or Tislelizumab in Patients with Metastatic Solid Tumors

Interventions

  • DRUG Tislelizumab
  • DRUG LYT-200
  • DRUG Gemcitabine/nab-paclitaxel

Study Locations (12)

Colorado

  • University of Colorado Hospital — Denver
  • Sarah Cannon Research Institute at Health One — Denver

Massachusetts

  • Massachusetts General Hospital — Boston
  • Beth Israel Deaconess Medical Center — Boston

New York

  • Columbia University — New York
  • Memorial Sloan-Kettering Cancer Center — New York

Texas

  • University of Texas, M.D. Anderson Cancer Center — Houston
  • South Texas Accelerated Research Therapeutics — San Antonio

California

  • UCLA — Los Angeles

Florida

  • Sarah Cannon Research Institute, Florida Cancer Specialists — Sarasota

Michigan

  • South Texas Accelerated Research Therapeutics — Grand Rapids

Tennessee

  • Sarah Cannon Research Institute, Tennessee Oncology — Nashville

Trial Details

FieldValue
Enrollment Target 44 participants
Start Date 2020-12-15
Est. Completion 2024-12-12
Phase Phase 1

Sponsor

PureTech

3 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04666688

The ClinicalTrials.gov registry entry for NCT04666688 describes a study currently listed as completed. 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 44 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is PureTech, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 6 conditions, with Colorectal Cancer appearing as the primary indexed condition, and to 3 interventions — of which Tislelizumab 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: NCT04666688 reports 12 study locations spanning 8 distinct geographic areas — top geographies include Colorado, Massachusetts, New York. 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 NCT04666688 about?

NCT04666688 is a clinical study titled "LYT-200 Alone and in Combination With Chemotherapy or Tislelizumab in Patients With Locally Advanced or Metastatic Solid Tumors". A Phase 1/2 Open-label, Multi-center Study of the Safety, Pharmacokinetics, and Anti-tumor Activity of LYT-200 Alone and in Combination with Chemotherapy or Tislelizumab in Patients with Metastatic Solid Tumors

What is the current status of trial NCT04666688?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 44 participants. The study started on 2020-12-15. Estimated completion is 2024-12-12.

What conditions does trial NCT04666688 study?

This clinical trial studies the following conditions: Colorectal Cancer, Pancreatic Cancer, Head and Neck Cancer, Solid Tumor, Metastatic Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04666688?

The interventions under investigation include: Tislelizumab (DRUG), LYT-200 (DRUG), Gemcitabine/nab-paclitaxel (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04666688?

This trial is sponsored by PureTech, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04666688 being conducted?

This trial has 12 study locations across California, Colorado, Florida, Massachusetts, Michigan. 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