Phase 2 Head and Neck Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- Adults aged 18 or older who are male, or female and neither pregnant nor breastfeeding
- People whose major organs (such as liver, kidneys, and bone marrow) are functioning adequately
- People who had previous cancer treatments (such as chemotherapy, biological therapy, hormone therapy, PARP inhibitors, or other oral or experimental drugs) where the last dose was received at least 4 weeks (or 6 weeks for certain specific drugs) or 5 half-lives before the trial starts — whichever comes first
- People whose side effects from previous cancer treatment, radiation, or surgery have mostly resolved to a mild level or better
- People with cancer that has spread to the brain, where that brain disease has been stable after radiation treatment
- People who had extensive radiation therapy (covering 30% or more of the bone marrow) must have finished that radiation at least 28 days before the trial starts; people who had more limited palliative radiation must have finished at least 14 days before
- People whose cancer can be measured on scans using standard criteria (RECIST v1.1), with scans taken within 4 weeks before the trial starts
- People with a general health and activity level rated as 0 or 1 on a standard medical scale, meaning fully active or able to carry out light activity (confirm with trial site)
- People whose doctors estimate they have a life expectancy of more than 12 weeks
- People who are willing and able to understand and sign an informed consent form
- Women who could potentially become pregnant and are sexually active with a non-sterilised male partner must be willing to use at least one highly effective form of contraception from screening until 5 half-lives plus 6 months after the last dose of the study drug, and must agree not to donate eggs or breastfeed during this period
- Male participants who are sexually active with a female partner who could potentially become pregnant must use an effective barrier contraceptive throughout treatment and until 5 half-lives plus 6 months after the last dose, and their partner should also use a highly effective method at the same time; male participants must also agree not to donate sperm for 6 months after the last dose
Who may not be able to join:
- No specific exclusion criteria were listed in the source information provided (confirm with trial site)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Yariv Houvras, MD, PhD, Tubulis GmbH
Phone: +491758005594
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Determination of MTD
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.