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NCT05310383
Tislelizumab and Radiotherapy for Recurrent Cervical Cancer
Phase 2 trial testing Tislelizumab plus radiotherapy in Recurrent Cervical Carcinoma in 58 participants. Status unknown.
27 March 2023
Quick facts
| Lead sponsor | Lei Li |
|---|---|
| Phase | Phase 2 |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 58 |
| Start date | 27 March 2022 |
| Primary completion | 27 March 2023 |
| Estimated completion | 27 March 2024 |
| Sites | 1 location across China |
Drugs / interventions tested
- Tislelizumab plus radiotherapy
Conditions studied
- Recurrent Cervical Carcinoma — all drugs for Recurrent Cervical Carcinoma →
- Metastatic Cervical Carcinoma — all drugs for Metastatic Cervical Carcinoma →
- Persistent Cervical Carcinoma — all drugs for Persistent Cervical Carcinoma →
- Radiotherapy — all drugs for Radiotherapy →
Sponsor
Lei Li — full company profile →
Who can join
18 and older, female only, with Recurrent Cervical Carcinoma or Metastatic Cervical Carcinoma. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This study is a prospective, multicenter, phase II clinical trial to evaluate the efficacy and safety of albumin-bound paclitaxel plus bevacizumab for platinum-resistant recurrent epithelial ovarian cancer. Patients with platinum-resistant recurrent ovarian cancer who meet the inclusion criteria, and don't meet any of the exclusion criteria, are enrolled in the study. They will receive albumin-bound paclitaxel (260 mg/m2) and bevacizumab (7.5mg/kg) intravenously every 21 days. The total treatment periods are no more than 6 cycles. Treatment continue until disease progression, intolerable toxicity, or patient refusal. Objective response rates primary objective. Progression-free survival, overall survival, and safety are secondary objectives. The study will enroll a total of 50 patients.
Publications & conference data
4 peer-reviewed publications reference this trial (live from Europe PMC):
-
Immune checkpoint inhibitors in cervical cancer: Current status and research progress.
Xie Y, Kong W, Zhao X, Zhang H, et al · · 2022 · cited 28× · PMID 36387196 · DOI 10.3389/fonc.2022.984896 -
Human papillomavirus associated cervical lesion: pathogenesis and therapeutic interventions.
Ye J, Zheng L, He Y, Qi X. · · 2023 · cited 27× · PMID 37719443 · DOI 10.1002/mco2.368 -
The abscopal effect of immune-radiation therapy in recurrent and metastatic cervical cancer: a narrative review.
Ollivier L, Moreau Bachelard C, Renaud E, Dhamelincourt E, et al · · 2023 · cited 6× · PMID 37539054 · DOI 10.3389/fimmu.2023.1201675 -
Bridging the Gap: Immune Checkpoint Inhibitor as an Option in the Management of Advanced and Recurrent Cervical Cancer in Sub-Saharan Africa.
Okpalanwaka IF, Anazodo FI, Chike-Aliozor ZL, Ekweozor C, et al · · 2024 · cited 2× · PMID 39398762 · DOI 10.7759/cureus.69136
Verify or expand the search:
- PubMed search for NCT05310383
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Recurrent Cervical Carcinoma
Currently open trials in the same condition.
- NCT06157151 — PRGN-2009 in Combination With Pembrolizumab Versus Pembrolizumab in Patients With Recurrent or Metastatic Cervical Cance · Phase 2 · recruiting
- NCT06238635 — Dostarlimab and Cobolimab in Advanced Cervical Cancer · Phase 2 · active not recruiting
- NCT04574635 — Human Papilloma Virus (HPV) Circulating Tumor DNA (ctDNA) in Cervical Cancer · active not recruiting
- NCT03968406 — Talazoparib and Radiation Therapy in Treating Patients With Locally Recurrent Gynecologic Cancers · Phase 1 · recruiting
- NCT02465060 — Targeted Therapy Directed by Genetic Testing in Treating Patients With Advanced Refractory Solid Tumors, Lymphomas, or M · Phase 2 · active not recruiting
Other Lei Li trials
Trials by the same sponsor.
- NCT06558019 — Exosome-based OCS Scores for Predicting Ovarian Cancer Recurrence · not yet recruiting
- NCT06557954 — Cervical Cytology DNA Methylation for Cervical Cancer Screening · not yet recruiting
- NCT05801263 — ctDNA Methylation for Epithelial Ovarian Cancer · unknown
- NCT05801276 — ctDNA Methylation for Detecting Ovarian Cancer · unknown
- NCT06490380 — HRD Status Reference Standard Based on WGS · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05310383 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Lei Li
- Last refreshed: 11 April 2022
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05310383.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing