Overview

A Study of AK104/Placebo Combined With Chemoradiotherapy For The Treatment of Locally Advanced Cervical Cancer

Status:
Not yet recruiting
Trial end date:
2029-05-01
Target enrollment:
0
Participant gender:
Female
Summary
This study is to evaluate the efficacy and safety of AK104 plus concurrent chemoradiotherapy compared to placebo plus concurrent chemoradiotherapy in participants with locally advanced cervical cancer
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Akeso
Treatments:
Cisplatin
Criteria
Inclusion Criteria:

1. signs the written informed consent form

2. ECOG 0-1

3. Life expectancy ≥ 3 months.

4. The histological types include squamous cell carcinoma,adenocarcinoma, or
adenosquamous cell carcinoma;

5. Locally advanced cervical cancer (LACC): The International Federation of Gynecology
and Obstetrics (FIGO) 2018 Stage 3A-4A

6. At least one measurable tumor lesion per RECIST v1.1

7. Adequate organ function as assessed in the laboratory tests

Exclusion Criteria:

1. Subjects with other histopathological types of cervical cancer, such as small cell
carcinoma, sarcoma, etc.

2. FIGO 2018 IVB

3. Subjects who had previously undergone total hysterectomy

4. Subjects who cannot receive brachytherapy

5. Subjects with other active malignancies within 2 years prior to randomization

6. Clinically significant hydronephrosis that cannot be relieved by nephrostomy or
ureteral stenting as judged by the Investigator

7. Any prior treatments targeting the mechanism of tumor immunity, such as immune
checkpoint inhibitors (e.g., anti-PD-1 antibody, anti-PDL1 antibody, anti-CTLA-4
antibody, etc.), or therapy against immune costimulatory factors (e.g., antibodies
directed against ICOS, CD40,CD137, GITR, OX40 targets, etc).

8. Subjects who require systemic treatment with glucocorticoid (>10 mg/day of prednisone
or equivalent glucocorticoid) or other immunosuppressive agents within 14 days prior
to randomization;

9. Major surgical treatment, open biopsy or significant trauma within 4 weeks prior to
randomization; or elective major surgical treatment required during the study

10. Use of live vaccines within 4 weeks prior to randomization

11. Active or potentially recurrent autoimmune disease

12. Known primary or secondary immunodeficiencies, including testing positive for human
immunodeficiency virus (HIV) antibodies

13. Known history of allogeneic organ transplantation and allogeneic hematopoietic stem
cell transplantation

14. Known history of interstitial lung disease or non-infectious pneumonitis

15. Pregnant or lactating women.

16. Any condition that, in the opinion of the Investigator, may result in a risk when
receiving the study drug.