Phase 2 Brain Cancer Trial, Recruiting NCT07505173 Sponsor: Tianjin Medical University Cancer Institute and Hospital Condition: Brain Cancer
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Phase 2 Brain Cancer Trial, Recruiting

NCT07505173
Recruiting Phase 2

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:

  • People who have given written consent to take part before enrolling
  • People aged between 18 and 75 years
  • People who have been diagnosed with a specific type of lung cancer called non-small cell lung adenocarcinoma, confirmed by laboratory tissue testing, and whose tumour has been confirmed to carry certain EGFR gene changes (specifically a deletion in exon 19 or a mutation called L858R in exon 21)
  • People who have cancer that has spread to the brain, confirmed by a contrast-enhanced CT or MRI scan, with between 1 and 10 brain tumour spots that may need targeted radiation, at least one brain spot measuring 10mm or more, and at least one measurable tumour spot outside the brain confirmed by appropriate imaging
  • People who are experiencing symptoms caused by their brain metastases
  • People whose general physical functioning is rated 0, 1, or 2 on a standard medical scale (ECOG), meaning they are able to carry out daily activities with no more than moderate limitation (confirm with trial site)
  • People whose doctors estimate they are likely to live at least 12 weeks or more
  • People who have not previously received any anti-cancer treatment for their lung cancer
  • People whose blood, liver, kidney, and heart function meet specific laboratory thresholds set by the trial (confirm with trial site for exact values)
  • People who are not surgically sterilised and women who could become pregnant must be using an approved method of contraception during treatment and for 3 months after treatment ends, and women who could become pregnant must have a negative pregnancy test within 7 days before enrolling and must not be breastfeeding
  • People who are willing to take part voluntarily, follow the study requirements, and attend safety and survival follow-up appointments

Who may not be able to join:

  • People who have uncontrolled fluid build-up in body cavities (such as around the lungs or in the abdomen) that cannot be managed by draining or other means
  • People who have conditions that would prevent them from taking oral medications properly, such as difficulty swallowing, previous removal of part of the digestive tract, ongoing severe diarrhoea, or bowel obstruction
  • People who are known to be pregnant, planning to become pregnant, or women who could become pregnant and are not willing to use effective contraception throughout the study
  • People who have serious other illnesses or who the trial doctor considers unsuitable for enrolment for any reason
  • People whose cancer has spread to the lining surrounding the brain and spinal cord (meningeal metastasis)
  • People who have taken part in another drug clinical trial within the 4 weeks before enrolling
  • People who are currently receiving any other anti-cancer treatment
  • People with a known history of misusing psychiatric medications, excessive alcohol use, or drug addiction
  • People with existing conditions that may interact with the study drugs, such as clinically significant heart rhythm abnormalities or active inflammatory lung disease
  • People whom the trial doctor considers unsuitable for any other reason that could affect their safety or ability to meet the study requirements

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 26 July 2026
Phase 2: approximately ~30% 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

Phone: 18622221203

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 2
Sponsor
Tianjin Medical University Cancer Institute and Hospital
Registry
ClinicalTrials.gov
Start date
1 January 2026
Est. completion
1 January 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Intracranial progression-free survival (iPFS )

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: 26 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