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NCT06707610 · ClinicalTrials.gov registry record · Phase 1

A Study to Evaluate the Safety, Tolerability, Pharmacokinetics (PK), and Antitumor Activity of ALK202 in Participants with Advanced Solid Tumors

A Phase 1 study of Advanced Solid Tumor and Advanced Cancer, sponsored by Shanghai Allink Biotherapeutics Co..

Recruiting
Registry status
Phase 1
Development phase
234
Enrollment target
4
Study locations

NCT06707610: Recruiting Phase 1 study of Advanced Solid Tumor and Advanced Cancer, sponsored by Shanghai Allink Biotherapeutics Co..

NCT06707610 is a Phase 1 study of Advanced Solid Tumor and Advanced Cancer that is actively recruiting participants, run by Shanghai Allink Biotherapeutics Co.. The registered enrollment target is 234 participants, above the 192-participant average among 189 other Advanced Solid Tumor trials with a reported enrollment target (22% higher). The trial reports 4 study locations across 3 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06707610, a Phase 1 study of Advanced Solid Tumor and Advanced Cancer, is actively recruiting participants, sponsored by Shanghai Allink Biotherapeutics Co..

RECRUITING
Registry status
Phase 1
Development phase
234 participants
Enrollment target
4
Study locations

Study Summary

TThis is a first-in-human (FIH), open-label, multicenter dose escalation and expansion study of ALK202. The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), and antitumor activity of ALK202 as a monotherapy in adult participants with Advanced Solid Tumors. The study will also identify recommended dose(s) for subsequent clinical studies of ALK202.

Primary Outcome

Dose-limiting toxicity (DLT); The incidence and severity of treatment-emergent adverse events (TEAEs) and treatment-related adverse events (TRAEs) according to CTCAE v5.0.

Interventions

  • DRUG ALK202

Study Locations (4)

New South Wales

  • Scientia Clinical Research Ltd - Randwick
  • Macquarie University - Sydney

Florida

  • D&H Cancer Research Center Llc - Margate

Virginia

  • Next Oncology - Fairfax

Trial Details

FieldValue
Enrollment Target 234 participants
Start Date 2025-02-10
Est. Completion 2028-12
Phase Phase 1

What NCT06707610 shows while recruiting

NCT06707610 is an interventional study that assigns participants to a tested intervention. The registered 234 participants enrollment target is mid-sized for trials with a published cap, above the 192-participant average among 189 other Advanced Solid Tumor trials with a reported enrollment target (22% higher).

The record links to 2 conditions, with Advanced Solid Tumor appearing as the primary indexed condition, and to 1 intervention - of which ALK202 is the first listed.

NCT06707610 reports a single indexed study location in New South Wales, Florida, Virginia.

Frequently Asked Questions

What is clinical trial NCT06707610 about?

NCT06707610 is a clinical study titled "A Study to Evaluate the Safety, Tolerability, Pharmacokinetics (PK), and Antitumor Activity of ALK202 in Participants with Advanced Solid Tumors". TThis is a first-in-human (FIH), open-label, multicenter dose escalation and expansion study of ALK202. The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), and antitumor activity of ALK202 as a monotherapy in adult participants with Advanced Solid Tumors. The st...

What is the current status of trial NCT06707610?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 234 participants. The study started on 2025-02-10. Estimated completion is 2028-12.

What conditions does trial NCT06707610 study?

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

What interventions are being tested in trial NCT06707610?

The interventions under investigation include: ALK202 (DRUG).

Who is sponsoring clinical trial NCT06707610?

This trial is sponsored by Shanghai Allink Biotherapeutics Co., which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06707610 being conducted?

This trial has 4 study locations across Florida, Virginia, New South Wales. 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 NCT06707610's enrollment target sits among peer trials

234 52nd of 189 higher than 137 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 NCT06707610, the US trial registry maintained by the National Library of Medicine. NCT06707610 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.