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NCT05525247 · ClinicalTrials.gov registry record · Phase 1

A Phase 1/2, Open-label, Multicenter, Dose Escalation and Expansion Study of SLC-3010 Monotherapy and in Combination

A Phase 1 study of Advanced Solid Tumor, sponsored by Selecxine.

Recruiting
Registry status
Phase 1
Development phase
420
Enrollment target
9
Study locations

NCT05525247 is a Phase 1 study of Advanced Solid Tumor that is actively recruiting participants, run by Selecxine. The registered enrollment target is 420 participants, above the 191-participant average among 189 other Advanced Solid Tumor trials with a reported enrollment target (120% higher). The trial reports 9 study locations across 9 states.

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The verdict

NCT05525247, a Phase 1 study of Advanced Solid Tumor, is actively recruiting participants, sponsored by Selecxine.

RECRUITING
Registry status
Phase 1
Development phase
420 participants
Enrollment target
9
Study locations

Study Summary

This is a Phase 1/2, open-label, multicenter, dose escalation and expansion study, evaluating the safety, tolerability, pharmacokinetic, preliminary anti-tumor activity, and effects on pharmacodynamic markers following administration of SLC-3010 as monotherapy and in combination with gemcitabine, in patients with various advanced solid tumors.

Conditions Studied

Interventions

  • DRUG SLC-3010
  • COMBINATION_PRODUCT Gemcitabine

Study Locations (9)

Florida

  • Selecxine Investigator site - Sarasota

Michigan

  • Selecxine Investigator site - Detroit

Oklahoma

  • Selecxine Investigator site - Oklahoma City

New South Wales

  • Selecxine Investigator site - Waratah

Perth

  • Selecxine Investigator site - Brentwood

Jongno-gu

  • Selecxine Investigator site - Seoul

Seodaemun-gu

  • Selecxine Investigator site - Seoul

Seongnam-si

  • Selecxine Investigator site - Gyeonggi-do

Trial Details

FieldValue
Enrollment Target 420 participants
Start Date 2022-12-21
Est. Completion 2028-01
Phase Phase 1

Sponsor

Selecxine

1 total trials

What the Registry Record Tells You About NCT05525247

The ClinicalTrials.gov registry entry for NCT05525247 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 420 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 191-participant average among 189 other Advanced Solid Tumor trials with a reported enrollment target (120% higher). The listed sponsor is Selecxine, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Advanced Solid Tumor appearing as the primary indexed condition, and to 2 interventions - of which SLC-3010 is the first listed.

NCT05525247 reports 9 study locations spanning 9 distinct geographic areas - top geographies include Florida, Michigan, Oklahoma.

Frequently Asked Questions

What is clinical trial NCT05525247 about?

NCT05525247 is a clinical study titled "A Phase 1/2, Open-label, Multicenter, Dose Escalation and Expansion Study of SLC-3010 Monotherapy and in Combination". This is a Phase 1/2, open-label, multicenter, dose escalation and expansion study, evaluating the safety, tolerability, pharmacokinetic, preliminary anti-tumor activity, and effects on pharmacodynamic markers following administration of SLC-3010 as monotherapy and in combination with gemcitabine, in...

What is the current status of trial NCT05525247?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 420 participants. The study started on 2022-12-21. Estimated completion is 2028-01.

What conditions does trial NCT05525247 study?

This clinical trial studies the following conditions: Advanced Solid Tumor.

What interventions are being tested in trial NCT05525247?

The interventions under investigation include: SLC-3010 (DRUG), Gemcitabine (COMBINATION_PRODUCT).

Who is sponsoring clinical trial NCT05525247?

This trial is sponsored by Selecxine, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05525247 being conducted?

This trial has 9 study locations across Florida, Michigan, Oklahoma, New South Wales, Perth. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

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