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

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. According to ClinicalTrials.gov, the official US trial registry.

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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.

Primary Outcome

Number of participants with DLTs of SLC-3010 treatment

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
Selecxine

1 total trials

What NCT05525247 shows while recruiting

NCT05525247 is an interventional study that assigns participants to a tested intervention. The registered 420 participants enrollment target is mid-sized for trials with a published cap, above the 191-participant average among 189 other Advanced Solid Tumor trials with a reported enrollment target (120% higher).

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 lists 9 locations in 9 states (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.

Similar trials for Advanced Solid Tumor

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05525247's enrollment target sits among peer trials

420 18th of 189 higher than 171 of 189 other Advanced Solid Tumor trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Advanced Solid Tumor trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05525247, the US trial registry maintained by the National Library of Medicine. NCT05525247 (mid enrollment · multi site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.