Clinical trial · Interventional
SHR-A1811 Combination Regimen for the Treatment of Recurrent or Metastatic Cervical Cancer
Open-label, Multicenter Phase Ib/II Clinical Study of Injectable SHR-A1811 in Combination Regimens for the Treatment of Recurrent or Metastatic Cervical Cancer
- 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 study is a multicentre, open-label, dose-finding/efficacy-expanding phase Ib/II clinical trial to evaluate the tolerability, safety, pharmacokinetic profile and immunogenicity of SHR-A1811 combination regimen in the treatment of recurrent or metastatic cervical cancer and to preliminarily evaluate the efficacy of SHR-A1811 combination regimen for recurrent or metastatic cervical cancer.
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 |
|---|---|---|---|
| Recurrent or Metastatic Cervical Cancer | — | UNRESOLVED | — |
Interventions
Interventions (6)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Adebelimab injection | Drug | — | UNRESOLVED |
| Bevacizumab injection | Drug | Bevacizumab | ALIAS |
| Carboplatin injection | Drug | Carboplatin | ALIAS |
| Cisplatin injection | Drug | Cisplatin | ALIAS |
| SHR-8068 | Drug | — | UNRESOLVED |
| SHR-A1811 | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- type
- EXPERIMENTAL
- label
- Treatment cohort 1
- interventionNames
- Drug: SHR-A1811
- Drug: Adebelimab injection
- Drug: Bevacizumab injection
- type
- EXPERIMENTAL
- label
- Treatment cohort 2
- interventionNames
- Drug: SHR-A1811
- Drug: Adebelimab injection
- Drug: Bevacizumab injection
- Drug: SHR-8068
- type
- EXPERIMENTAL
- label
- Treatment cohort 3
- interventionNames
- Drug: SHR-A1811
- Drug: Adebelimab injection
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: 1. Subjects must voluntarily join this study, sign the informed consent form, have good compliance and be able to cooperate with the follow-up. 2. Female, aged 18-75 years old. 3. Expected survival ≥ 12 weeks. 4. Normal function of vital organs. 5. Female subjects of childbearing potential must have a negative serum HCG test within 7 days prior to the first dose and must be non-lactating. 6. Female subjects must agree to comply with contraceptive requirements from signing the informed consent form to 7 months after the last dose of the investigational drug. Exclusion Criteria: 1. Previous or concomitant other malignancies. 2. Severe bone damage caused by bone metastasis from tumours. 3. Presence of active autoimmune disease or history of autoimmune disease with possible recurrence. 4. Those with active tuberculosis. 5. Concomitant poorly controlled or severe cardiovascular disease. 6. Occurrence of arteriovenous thrombotic events within 6 months prior to the first dose. 7. Presence of gastrointestinal obstruction or presence of symptoms and signs of gastrointestinal obstruction within 6 months prior to the first dose. 8. Subjects who have had a serious infection within 1 month before the first dose. 9. Subjects who have a history of immunodeficiency. 10. As judged by the investigator, there are other factors that may affect the results of the study or cause the study to be forced to terminate halfway.
References
Publications (0)
Data not yet available