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NCT04903873 · ClinicalTrials.gov registry record · Phase 1
A Study to Evaluate Safety, Efficacy, and Pharmacokinetics in Participants With Advanced Solid Tumors
A Phase 1 study of Prostate Cancer and Non-Small Cell Lung Cancer, sponsored by Eutilex.
- Recruiting
- Registry status
- Phase 1
- Development phase
- 110
- Enrollment target
- 6
- Study locations
NCT04903873 is a Phase 1 study of Prostate Cancer and Non-Small Cell Lung Cancer that is actively recruiting participants, run by Eutilex. The registered enrollment target is 110 participants, below the 608-participant average among 735 other Prostate Cancer trials with a reported enrollment target (82% lower). The trial reports 6 study locations across 3 states.
The verdict
NCT04903873, a Phase 1 study of Prostate Cancer and Non-Small Cell Lung Cancer, is actively recruiting participants, sponsored by Eutilex.
- RECRUITING
- Registry status
- Phase 1
- Development phase
- 110 participants
- Enrollment target
- 6
- Study locations
Study Summary
Phase 1 (Dose Escalation) of this study will assess the safety, tolerability, dose-limiting toxicity (DLT), and will determine the maximum tolerated dose (MTD) and recommended Phase 2 dose (RP2D) of EU101 in participants with advanced solid tumors. Phase 2 (Dose Expansion) of the study will assess the antitumor effect of EU101 in two indications including colorectal cancer (CRC) and non-small cell lung cancer (NSCLC).
Conditions Studied
Interventions
- DRUG EU101
Study Locations (6)
Other
- National Cancer Center - Ilsan
- Samsung Seoul Hospital - Seoul
- Seoul Asan - Seoul
- Severance Hospital - Seoul
Pennsylvania
- Fox Chase Cancer Center - Philadelphia
Texas
- Mary Crowley Center - Dallas
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 110 participants |
| Start Date | 2021-05-31 |
| Est. Completion | 2025-12 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04903873
The ClinicalTrials.gov registry entry for NCT04903873 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 110 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 608-participant average among 735 other Prostate Cancer trials with a reported enrollment target (82% lower). The listed sponsor is Eutilex, which has 1 total studies on file at ClinicalTrials.gov.
The record links to 5 conditions, with Prostate Cancer appearing as the primary indexed condition, and to 1 intervention - of which EU101 is the first listed.
NCT04903873 reports 6 study locations spanning 3 distinct geographic areas - top geographies include Other, Pennsylvania, Texas.
Frequently Asked Questions
What is clinical trial NCT04903873 about?
NCT04903873 is a clinical study titled "A Study to Evaluate Safety, Efficacy, and Pharmacokinetics in Participants With Advanced Solid Tumors". Phase 1 (Dose Escalation) of this study will assess the safety, tolerability, dose-limiting toxicity (DLT), and will determine the maximum tolerated dose (MTD) and recommended Phase 2 dose (RP2D) of EU101 in participants with advanced solid tumors. Phase 2 (Dose Expansion) of the study will assess t...
What is the current status of trial NCT04903873?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 110 participants. The study started on 2021-05-31. Estimated completion is 2025-12.
What conditions does trial NCT04903873 study?
This clinical trial studies the following conditions: Prostate Cancer, Non-Small Cell Lung Cancer, Solid Tumor, Renal Cell Carcinoma, Renal Cell Cancer Metastatic.
What interventions are being tested in trial NCT04903873?
The interventions under investigation include: EU101 (DRUG).
Who is sponsoring clinical trial NCT04903873?
This trial is sponsored by Eutilex, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04903873 being conducted?
This trial has 6 study locations across Pennsylvania, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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