Clinical trial · Interventional
Phase 1 Study of Pemigatinib in Patients With Advanced Malignancies With FGF/FGFR Alterations
A Phase 1, Open-Label, Pharmacokinetic(PK), Pharmacodynamics(PD) and Safety Study of Pemigatinib in Patients With Advanced Malignancies With FGF/FGFR Alterations
NCT04258527CI-TRIAL-00052879completedPhase 1ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This is a phase 1 study to investigate the characteristics of PK, PD and safety in subjects with advanced malignancies with FGF/FGFR alterations.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Solid Tumor | Solid Neoplasm | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Pemigatinib | Drug | Pemigatinib | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Patients with advanced malignancies with FGF/FGFR alterations
- interventionNames
- Drug: Pemigatinib
Primary outcomes (3)
- measure
- Maximum observed plasma concentration (Cmax) during the dosing interval and Cmin of Pemigatinib as monotherapy
- timeFrame
- Day 1 to Day 16
- measure
- Time to maximum plasma concentration (Tmax) of Pemigatinib as monotherapy
- timeFrame
- Day 1 to Day 16
- measure
- Area under the single-dose plasma concentration-time curve (AUC0-t) of Pemigatinib as monotherapy
- timeFrame
- Day 1 to Day 16
Secondary outcomes (1)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Men and women, aged 18 or older. 2. Histologically or cytologically confirmed malignancy which was considered to be surgically unresectable advanced, relapse or metastatic . 3. Radiographically measurable disease per RECIST v 1.1 4. Documentation of FGF/FGFR alteration.. 5. Documented disease progression after standard therapy ,or no standard therapy available. 6. ECOG performance status of 0\~1. 7. Life expectancy ≥12 weeks Exclusion Criteria: 1. Prior receipt of a selective FGFR inhibitor. 2. History of calcium and phosphate hemostasis disorder or systemic mineral imbalance with ectopic calcification of softy tissues ( exception: skin, kidney, tendons or vessels due to injury, disease, and aging, in the absence of systemic mineral imbalance). 3. Currently evidence of clinically significant corneal or retinal disorder confirmed by ophthalmologic examination. 4. Use of any potent CYP3A4 inhibitors or inducers within 14 days or 5 half-lives, whichever is shorter, before the first dose of study drug. Topical ketoconazole will be allowed
References
Publications (1)
- DERIVEDDeng T, Zhang L, Shi Y, Bai G, Pan Y, Shen A, Han X, Yang Z, Chen M, Zhou H, Luo Y, Zheng S, Ba Y. Pharmacokinetics, pharmacodynamics and efficacy of pemigatinib (a selective inhibitor of fibroblast growth factor receptor 1-3) monotherapy in Chinese patients with advanced solid tumors: a phase i clinical trial. Invest New Drugs. 2023 Dec;41(6):808-815. doi: 10.1007/s10637-023-01396-x. Epub 2023 Oct 27. PMID 37889382