A Study of 3HP-2827 in Treatment of Unresectable or Metastatic Solid Tumors With FGFR2 Alterations
Recruiting now · Phase 1/Phase 2
Conditions studied: Solid Tumors With FGFR2 Alterations, Adult
In brief
The study is being conducted to evaluate the safety, tolerability, efficacy, pharmacokinetics, and pharmacodynamics of 3HP-2827 in the treatment of unresectable or metastatic solid tumors with FGFR2 alterations.
Key facts
- Study ID
- NCT06378593
- Run by
- 3H (Suzhou) Pharmaceuticals Co., Ltd.
- People needed
- 130
- Starts
- 2024-06-17
- Expected to finish
- 2028-06-16
- Last updated by the study team
- 2026-01-27
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- The patient is willing and able to provide written informed consent and has the ability to comply with the study protocol
- Men or women, age ≥ 18 years at the time of signing informed consent.
- Histologically or cytologically confirmed surgically unresectable, locally advanced, metastatic solid tumor.
- ECOG score is 0 or 1.
- An expected survival of ≥ 12 weeks.
- Evaluable or measurable disease per RECIST v1.1.
- Adequate organ function, as measured by laboratory values.
You may not qualify if…
- Active brain metastases.
- Have other malignancies within the past 3 years.
- The toxicity from previous anti-tumor treatment has not recovered to ≤ grade 1.
- Clinically significant corneal or retinal disease/keratopathy.
- Clinically significant cardiovascular disorders.
- Failure to swallow, chronic diarrhea, or presence of other factors affecting drug absorption.
- Known to be allergic to any study drug or any of its excipients.
- Assessed by the investigator to be unsuitable for participation in this study.
Where it is running
- Beijing Cancer Hospital — Beijing, Beijing Municipality, China (enrolling)
- ZhongShan Hospital — Shanghai, Shanghai Municipality, China (enrolling)
Full record on ClinicalTrials.gov
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