Phase 2 Brain 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 between 18 and 75 years old (male or female)
- People who have been newly diagnosed with glioblastoma (a type of brain tumour), confirmed by a scan or tissue test, where at least 80% of the tumour was surgically removed
- People who have completed a combined chemotherapy and radiation treatment (called CCRT) no less than 4 weeks and no more than 6 weeks before joining the study
- People who have been on a stable or decreasing dose of steroid medication for more than 2 weeks
- People with a Karnofsky score of 70 or above — this is a measure doctors use to assess a person's general ability to carry out daily activities (confirm with trial site)
- People with a life expectancy of more than 12 weeks
- People whose blood and organ function results are within acceptable ranges (confirm with trial site for specific requirements)
- People who agree to use adequate contraception during the study and for 6 months after the last dose of the study treatment
- People who are willing and able to sign a consent form before any study procedures begin
- People whose tumour has a specific genetic feature called MGMT unmethylation — this applies only to a particular group within the trial called the Dose Expansion Cohort (confirm with trial site)
Who may not be able to join:
- People who have already received any cancer treatment other than the combined chemotherapy and radiation treatment (CCRT)
- People whose primary tumour is located in the brain stem or spinal cord
- People who have had a severe allergic reaction to any ingredient in the study drug, JK-1201I
- People who have had serious, uncontrolled, or active heart or blood vessel disease in the past 6 months
- People who are unable to swallow tablets or capsules, or who have significant digestive system problems that could affect how the study drug is absorbed
- People who have seizures that are not well controlled
- People who are currently taking certain medications that cannot be stopped at least 2 weeks before starting the study treatment
- People with severe or uncontrolled high blood pressure
- People who still have unresolved side effects from a previous cancer treatment
- Women who are pregnant or breastfeeding
- People who have tested positive for HIV, or who have an active hepatitis B or hepatitis C infection
- People who have taken part in another clinical trial within the 4 weeks before signing the consent form
- People with a history of mental health disorders
- People whom the trial doctor considers unsuitable to participate for any other reason
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
Phone: 8610-82156767
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
Incidence and Grade of Participants with Adverse Events or Serious Adverse Events
Can't join this trial?
Data last synced from ClinicalTrials.gov: 22 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.