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NCT04505839 · ClinicalTrials.gov registry record · Phase 1

First-In-Human Dose-Escalation Study of STP1002 in Patients With Advanced-Stage Solid Tumors

A Phase 1 study, sponsored by ST Pharm Co..

Completed
Registry status
Phase 1
Development phase
32
Enrollment target

NCT04505839: Completed Phase 1 study, sponsored by ST Pharm Co..

NCT04505839 is a Phase 1 study that has completed, run by ST Pharm Co.. The registered enrollment target is 32 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (47% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04505839, a Phase 1 study, has completed, sponsored by ST Pharm Co..

COMPLETED
Registry status
Phase 1
Development phase
32 participants
Enrollment target

Study Summary

This is an open-label, multicenter, dose-escalation study to evaluate the safety, tolerability, and pharmacokinetics (PK) and to determine the maximum tolerated dose (MTD) of STP1002 in patients with advanced-stage solid tumors.

Primary Outcome

DLTs are defined as any of the following adverse events (AEs) that are possibly or probably related to the trial regimen occurring during Cycle 1

Interventions

  • DRUG STP1002

Trial Details

FieldValue
Enrollment Target 32 participants
Start Date 2020-07-30
Est. Completion 2023-03-07
Phase Phase 1
ST Pharm Co.

2 total trials

What the finished NCT04505839 record still lists

NCT04505839 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 32 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (47% lower).

The record links to 0 conditions, and to 1 intervention - of which STP1002 is the first listed.

NCT04505839 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04505839 about?

NCT04505839 is a clinical study titled "First-In-Human Dose-Escalation Study of STP1002 in Patients With Advanced-Stage Solid Tumors". This is an open-label, multicenter, dose-escalation study to evaluate the safety, tolerability, and pharmacokinetics (PK) and to determine the maximum tolerated dose (MTD) of STP1002 in patients with advanced-stage solid tumors.

What is the current status of trial NCT04505839?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 32 participants. The study started on 2020-07-30. Estimated completion is 2023-03-07.

What interventions are being tested in trial NCT04505839?

The interventions under investigation include: STP1002 (DRUG).

Who is sponsoring clinical trial NCT04505839?

This trial is sponsored by ST Pharm Co., which has 2 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04505839's enrollment target sits among peer trials

32 1296th of 2000 higher than 679 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT04505839, the US trial registry maintained by the National Library of Medicine. NCT04505839 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.