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

ACTIVE NOT RECRUITING Phase 1

Debio 0123 in Combination With Carboplatin and Etoposide in Adult Participants With Small Cell Lung Cancer That Recurred or Progressed After Previous Standard Platinum-Based Therapy

NCT05815160 · View on ClinicalTrials.gov ↗

Study Summary

The primary purpose of part 1 (dose escalation) of this study is to identify the recommended dose and to characterize the safety and tolerability of Debio 0123 in combination with carboplatin and etoposide. The primary purpose of part 2 (dose expansion) of this study is to characterize the safety and tolerability of Debio 0123 at the recommended dose when administered in combination with carboplatin and etoposide.

Interventions

  • DRUG Carboplatin
  • DRUG Etoposide
  • DRUG Debio 0123

Study Locations (13)

Other

  • Hospital Universitario de A Coruna — A Coruña
  • Hospital Universitario Vall d'Hebron — Barcelona
  • Hospital Clinic Barcelona — Barcelona
  • Institut Catala D'Oncologia - Badalona — Barcelona
  • Clinica Universidad de Navarra — Madrid
  • Hospital Universitario 12 de Octubre — Madrid
  • Hospital Universitario HM Sanchinarro. START Madrid - Centro Integral Oncológico Clara Campal (CIOCC) — Madrid
  • NEXT Oncology Madrid — Madrid
  • Hospital Quironsalud Malaga — Málaga
  • Clinica Universidad de Navarra — Pamplona
  • Hospital Clinico Universitario de Valencia — Valencia

Arkansas

  • University of Arkansas for Medical Sciences — Little Rock

New York

  • Roswell Park Comprehensive Cancer Center — Buffalo

Trial Details

FieldValue
Enrollment Target 34 participants
Start Date 2023-05-02
Est. Completion 2026-03
Phase Phase 1

Sponsor

Debiopharm International

41 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05815160

The ClinicalTrials.gov registry entry for NCT05815160 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 34 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Debiopharm International, which has 41 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 Small Cell Lung Cancer Recurrent appearing as the primary indexed condition, and to 3 interventions — of which Carboplatin 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: NCT05815160 reports 13 study locations spanning 3 distinct geographic areas — top geographies include Other, Arkansas, 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 NCT05815160 about?

NCT05815160 is a clinical study titled "Debio 0123 in Combination With Carboplatin and Etoposide in Adult Participants With Small Cell Lung Cancer That Recurred or Progressed After Previous Standard Platinum-Based Therapy". The primary purpose of part 1 (dose escalation) of this study is to identify the recommended dose and to characterize the safety and tolerability of Debio 0123 in combination with carboplatin and etoposide. The primary purpose of part 2 (dose expansion) of this study is to characterize the safety a...

What is the current status of trial NCT05815160?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 34 participants. The study started on 2023-05-02. Estimated completion is 2026-03.

What conditions does trial NCT05815160 study?

This clinical trial studies the following conditions: Small Cell Lung Cancer Recurrent. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05815160?

The interventions under investigation include: Carboplatin (DRUG), Etoposide (DRUG), Debio 0123 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05815160?

This trial is sponsored by Debiopharm International, which has 41 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05815160 being conducted?

This trial has 13 study locations across Arkansas, New York. 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