Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06770764 · ClinicalTrials.gov registry record · Phase 1

Dose Escalation and Expansion Study Evaluating ODC-IL2 in Adult Patients With Advanced or Metastatic Solid Tumors

A Phase 1 study of Advanced Solid Tumors and Metastatic Solid Tumors, sponsored by Trutino Biosciences.

Recruiting
Registry status
Phase 1
Development phase
50
Enrollment target
1
Study location

NCT06770764: Recruiting Phase 1 study of Advanced Solid Tumors and Metastatic Solid Tumors, sponsored by Trutino Biosciences.

NCT06770764 is a Phase 1 study of Advanced Solid Tumors and Metastatic Solid Tumors that is actively recruiting participants, run by Trutino Biosciences. The registered enrollment target is 50 participants, below the 198-participant average among 144 other Advanced Solid Tumors trials with a reported enrollment target (75% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06770764, a Phase 1 study of Advanced Solid Tumors and Metastatic Solid Tumors, is actively recruiting participants, sponsored by Trutino Biosciences.

RECRUITING
Registry status
Phase 1
Development phase
50 participants
Enrollment target
1
Study location

Study Summary

This is a first-in-human, Phase I, multicenter, open-label, dose escalation study with dose expansion to evaluate the safety and antitumor activity of ODC-IL2 in patients with advanced or metastatic solid tumors. ODC-IL2 is a conditionally activated IL-2 prodrug and will be administered as a single agent via intravenous infusion on Days 1 and 15 of a 28-day cycle. Up to approximately 50 patients will be enrolled in this study.

Interventions

  • DRUG ODC-IL2

Study Locations (1)

Arizona

  • HonorHealth - Scottsdale

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2024-12-30
Est. Completion 2027-03
Phase Phase 1
Trutino Biosciences

1 total trials

What NCT06770764 shows while recruiting

NCT06770764 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 198-participant average among 144 other Advanced Solid Tumors trials with a reported enrollment target (75% lower).

The record links to 2 conditions, with Advanced Solid Tumors appearing as the primary indexed condition, and to 1 intervention - of which ODC-IL2 is the first listed.

NCT06770764 reports a single indexed study location in Arizona.

Frequently Asked Questions

What is clinical trial NCT06770764 about?

NCT06770764 is a clinical study titled "Dose Escalation and Expansion Study Evaluating ODC-IL2 in Adult Patients With Advanced or Metastatic Solid Tumors". This is a first-in-human, Phase I, multicenter, open-label, dose escalation study with dose expansion to evaluate the safety and antitumor activity of ODC-IL2 in patients with advanced or metastatic solid tumors. ODC-IL2 is a conditionally activated IL-2 prodrug and will be administered as a single ...

What is the current status of trial NCT06770764?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 50 participants. The study started on 2024-12-30. Estimated completion is 2027-03.

What conditions does trial NCT06770764 study?

This clinical trial studies the following conditions: Advanced Solid Tumors, Metastatic Solid Tumors.

What interventions are being tested in trial NCT06770764?

The interventions under investigation include: ODC-IL2 (DRUG).

Who is sponsoring clinical trial NCT06770764?

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

Where is trial NCT06770764 being conducted?

This trial has 1 study location across Arizona. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Advanced Solid Tumors

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 NCT06770764's enrollment target sits among peer trials

50 100th of 144 higher than 44 of 144 other Advanced Solid Tumors trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Advanced Solid Tumors 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00200889 · 50 participants · Early Phase 1

    Mapping Auricular Vagus Nerve Circuitry

  • NCT00409435 · 50 participants · Phase 2

    A Study of Pyridostigmine in Postural Tachycardia Syndrome

  • NCT01202305 · 50 participants

    The Use of Lymph Node Biopsies to Support HIV Pathogenesis Studies

  • NCT01225913 · 50 participants · Phase 4

    Mechanism(s) of Airflow Limitation During Exacerbation of Asthma

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06770764, the US trial registry maintained by the National Library of Medicine. NCT06770764 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.