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Taking people in SpainPhase 1/2

Tests TH9619 in adults with advanced solid tumors

Tests the drug TH9619 in adults with advanced solid cancers.

Plain-language title generated from the registry record
Registry title: Phase 1/2 Study to Evaluate TH9619 in the Treatment of Advanced Solid Tumors

Key facts

Where
Barcelona and Madrid, SpainSee the 2 sites
Phase
Phase 1/2

Where in Spain

  • Vall d'Hebron Institute of OncologyBarcelona, SpainTaking people
  • Hospital Universitario Fundación Jiménez DíazMadrid, SpainTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
One-carbon Therapeutics AB
Trial code
NCT07151040EU 2024-519639-40-00
Record updated
28 January 2026
Original description
This is a first in human, multi-center, open-label, dosage escalation study to determine the recommended dose range of TH9619 in subjects with advanced cancer.Read full original descriptionShow less

A First-in-human, Phase 1/2, Multicenter, Open-label, Dose Escalation, Confirmation and Expansion Study to Evaluate the Safety, Pharmacokinetics and Antitumor Activity of TH9619 in Subjects With Advanced Solid Tumors

This is a first in human, multi-center, open-label, dosage escalation study to determine the recommended dose range of TH9619 in subjects with advanced cancer.

Inclusion: Must have given written informed consent; Histopathologically confirmed advanced cancer (colorectal cancer, head and neck squamous cell cancer, non-small cell lung cancer and gastric cancer (including gastroesophageal junction cancer)); Prior treatment with at least one line of cytotoxic systemic therapy for metastatic/unresectable cancer; Adult patients (≥18 years of age); Must be willing to comply with study procedures.

Exclusion: History or presence of any clinically significant disorders as judged by the Investigator.

ClinicalTrials.gov NCT07151040 · EU CTIS 2024-519639-40-00