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NCT05189171: MODEL-CRC

MicroOrganoSphere (MOS) Drug Screen Pilot Trial in Colorectal Cancer

Completed Last updated 28 June 2024
What this trial tests

trial testing MicroOrganoSphere (MOS) drug screen in Colorectal Neoplasms in 46 participants. Completed in 18 March 2024.

Timeline
25 October 2022
Primary endpoint
3 November 2023
18 March 2024

Quick facts

Lead sponsorXilis, Inc.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment46
Start date25 October 2022
Primary completion3 November 2023
Estimated completion18 March 2024
Sites7 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Xilis, Inc.

Who can join

18 and older, any sex, with Colorectal Neoplasms. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of the study is to determine the feasibility of generating sufficient MicroOrganoSpheres (MOS) from a biopsy of a subject's adenocarcinoma of the colon and/or rectum that is metastatic to the liver and completing a drug screen against patient-derived MOS using standard of care drugs used in the treatment of colorectal cancer (oxaliplatin, irinotecan, 5-FU/capecitabine (Xeloda), bevacizumab, panitumumab or cetuximab, trifluridine/tipiracil (Lonsurf), regorafenib and pembrolizumab or nivolumab) in ≤ 14 days.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Patient-derived micro-organospheres enable clinical precision oncology.
    Ding S, Hsu C, Wang Z, Natesh NR, et al · · 2022 · cited 148× · PMID 35508177 · DOI 10.1016/j.stem.2022.04.006

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Other recruiting trials for Colorectal Neoplasms

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05189171.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing