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NCT05001516 · ClinicalTrials.gov registry record · Phase 1

Study of Turning Point Therapeutics LM-302 in Patients With Advance Solid Tumors

A Phase 1 study, sponsored by Turning Point Therapeutics.

Completed
Registry status
Phase 1
Development phase
17
Enrollment target

NCT05001516: Completed Phase 1 study, sponsored by Turning Point Therapeutics.

NCT05001516 is a Phase 1 study that has completed, run by Turning Point Therapeutics. The registered enrollment target is 17 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (72% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05001516, a Phase 1 study, has completed, sponsored by Turning Point Therapeutics.

COMPLETED
Registry status
Phase 1
Development phase
17 participants
Enrollment target

Study Summary

A Phase I, First-in-Human, Open-Label, Dose Escalation and Expansion Study of LM-302 in Patients with CLDN18.2-Positive Advanced Solid Tumors

Primary Outcome

DLT is defined as a toxicity (adverse event at least possibly related to LM302) occurring during the DLT observation period

Interventions

  • DRUG LM-302

Trial Details

FieldValue
Enrollment Target 17 participants
Start Date 2021-12-29
Est. Completion 2024-01-04
Phase Phase 1
Turning Point Therapeutics

7 total trials

What the finished NCT05001516 record still lists

NCT05001516 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 17 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (72% lower).

The record links to 0 conditions, and to 1 intervention - of which LM-302 is the first listed.

NCT05001516 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05001516 about?

NCT05001516 is a clinical study titled "Study of Turning Point Therapeutics LM-302 in Patients With Advance Solid Tumors". A Phase I, First-in-Human, Open-Label, Dose Escalation and Expansion Study of LM-302 in Patients with CLDN18.2-Positive Advanced Solid Tumors

What is the current status of trial NCT05001516?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 17 participants. The study started on 2021-12-29. Estimated completion is 2024-01-04.

What interventions are being tested in trial NCT05001516?

The interventions under investigation include: LM-302 (DRUG).

Who is sponsoring clinical trial NCT05001516?

This trial is sponsored by Turning Point Therapeutics, which has 7 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05001516's enrollment target sits among peer trials

17 1785th of 2000 higher than 215 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 NCT05001516, the US trial registry maintained by the National Library of Medicine. NCT05001516 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.