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NCT05815862
NCT05815862
Who may be able to join
Who might be able to join this trial:
- You have been diagnosed with advanced lung cancer or ovarian cancer, confirmed by a lab test of tissue or cell samples
- You are between 18 and 75 years old at the time of signing the consent form
- You are generally able to carry out light activity and care for yourself (your doctor will assess this using a standard scale)
- You have at least one tumour that can be measured on a scan
- Your major organs (such as liver, kidneys, and heart) are working normally
- If you are a woman who could become pregnant, you have a negative pregnancy test within 7 days before joining, you are not breastfeeding, and you agree to use contraception during the study and for 6 months after it ends
- If you are a man, you agree to use contraception during the study and for 6 months after it ends
- You are willing to take part voluntarily and sign a consent form, and are able to follow the study requirements
Who may not be able to join:
- You have had or currently have another type of cancer within the last 3 years
- You are unable to take oral (swallowed) medication for any reason
- You still have side effects from a previous cancer treatment that have not fully resolved (beyond minor hair loss)
- You had major surgery or a serious injury within 4 weeks before starting the study
- You have unhealed wounds, broken bones, active stomach or small intestine ulcers, persistent blood in your stool, ulcerative colitis, or other conditions that could cause serious gut bleeding or tearing
- You have had a stroke, mini-stroke, blood clot in a deep vein, or a blood clot in the lungs within the 6 months before starting the study
- You have a history of substance abuse involving mind-altering drugs and are unable to stop, or you have a mental health disorder
- You have any severe or uncontrolled illness (confirm with trial site)
- You received chemotherapy, radiotherapy, or other cancer treatments within 4 weeks before starting the study
- You received certain traditional Chinese medicines with anti-cancer properties within 2 weeks before starting the study
- You have previously been treated with specific anti-cancer drugs that target blood vessel growth, including Cabozantinib, Anlotinib, Endostar, or Bevacizumab
- Scans show that the tumour has grown into major blood vessels, or the study doctor thinks there is a high risk of serious bleeding from blood vessels
- You have a history of lung scarring, severe lung damage, severe radiation-related lung injury, drug-related lung disease, or scans show active severe lung inflammation
- You have fluid build-up around the lungs, in the abdomen, or around the heart that is uncontrolled and needs repeated draining
- You have cancer that has spread to the brain with active symptoms, or symptoms that have only been controlled for less than 2 weeks
- You have taken part in another clinical trial using an experimental cancer drug within the 4 weeks before starting this study
- You have a type of lung cancer (central squamous cell carcinoma) that carries a high risk of coughing up blood
- Your doctor believes you have another condition that could put your safety at risk or prevent you from completing the study
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.
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.
Trial details
Status
Completed
Phase
Phase 2
Sponsor
Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
Registry
clinicaltrials_gov
Start date
15 February 2023
Est. completion
20 August 2025
Where this trial is recruiting
🇨🇳 China
Primary endpoints
Objective remission rate (ORR); Progression free survival (PFS)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.