Phase 1 Brain Cancer Trial, Recruiting NCT06641908 Sponsor: EMD Serono Research & Development Institute, Inc. Condition: Brain Cancer
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Phase 1 Brain Cancer Trial, Recruiting

NCT06641908
Recruiting Phase 1

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:

  • Group A (Soft Tissue Sarcoma): People who have been diagnosed with a type of cancer called soft tissue sarcoma (STS) that has spread or cannot be surgically removed, and whose cancer has gotten worse after at least one previous treatment that included a drug from the anthracycline family of chemotherapy drugs.
  • People whose cancer could be operated on but still had cancer remaining after surgery may be considered, provided the surgery took place at least 4 weeks before starting the trial treatment.
  • Group B (Brain Cancer): People who have been diagnosed with a specific type of brain tumour called glioblastoma (IDH-wildtype) that has come back after receiving exactly one previous treatment (which included radiation therapy, with or without a drug called temozolomide, depending on their tumour type), and whose cancer returned at least 3 months after finishing radiation therapy.
  • People who are in reasonably good general health, as measured by a standard scale called the ECOG Performance Status — specifically, those with a score of 0 or 1 (meaning able to carry out normal daily activities with little or no restriction).
  • People whose blood, liver, and kidney function meet the levels required by the trial protocol.
  • There may be additional requirements set out in the full trial protocol (confirm with trial site).

Who may not be able to join:

  • People who have had a different type of cancer (other than soft tissue sarcoma or glioblastoma, depending on which group applies) within the past 3 years — though some exceptions may apply, such as certain skin cancers, early-stage cervical changes, benign prostate conditions, or cancers that the treating doctor considers to be fully resolved with very low chance of returning.
  • Soft tissue sarcoma group only: People who have had cancer spread to the brain, to the lining surrounding the brain or spinal cord, or who have pressure on the spinal cord.
  • There may be additional reasons a person would not be eligible, as set out in the full trial protocol (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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
Phase 1: approximately ~10% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Medical Responsible, EMD Serono Research & Development Institute, Inc.

Phone: 888-275-7376

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

Status
Recruiting
Phase
Phase 1
Sponsor
EMD Serono Research & Development Institute, Inc.
Registry
ClinicalTrials.gov
Start date
8 November 2024
Est. completion
16 April 2027

Where this trial is recruiting

🇧🇪 Belgium 🇫🇷 France 🇯🇵 Japan 🇨🇭 Switzerland 🇬🇧 United Kingdom 🇺🇸 United States

Primary endpoints

Number of Participants with Dose Limiting Toxicities (DLTs) and Adverse Events (AEs)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov