A Study of QL1706 Combined with Nine HPV Vaccine As First-line Treatment for Persistent, Recurren… (NCT06882447) | Clinical Trial Compass
Not Yet RecruitingPhase 2
A Study of QL1706 Combined with Nine HPV Vaccine As First-line Treatment for Persistent, Recurrent or Metastatic Cervical Cancer
35 participantsStarted 2025-03
Plain-language summary
The study medications were used as follows: 1 cycle every 21 days (3 weeks) of the following regimen.
Test drug: QL1706, HPV 9-valent vaccine
QL1706: Dose: 5 mg/kg ; intravenous infusion (ivgtt), administered on Day 1 of each cycle and every 3 weeks (21 days).
Treatment will continue until loss of clinical benefit, occurrence of intolerable toxicity, patient or physician decision to discontinue treatment, death of the patient receiving the experimental treatment, or completion of 2 years of dosing (35 dosing cycles), withdrawal of informed consent by the subject, pregnancy of the subject, noncompliance with protocol or procedural requirements, or for administrative reasons.
HPV 9-valent vaccine: 1st dose 1 day prior to first QL1706 administration; 2nd dose 2 months after 1st dose; 3rd dose 6 months after 1st dose.
Who can participate
SexFEMALE
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1. Patients with unsystematically treated cervical cancer, who voluntarily participate in the clinical study; fully understand and informed about the study and sign the Informed Consent Form (ICF); willing to follow and have the ability to complete all the trial procedures.
2. With histologically confirmed diagnosis of cervical cancer, a pathology report and pathology slides are required.
3. have at least one measurable lesion as assessed by the investigator according to RECIST 1.1.
Note: Measurable target lesions cannot be selected from previous radiotherapy sites. If the target lesion at the site of prior radiotherapy is the only optional target lesion, the investigator is required to provide anterior and posterior imaging data showing significant progression of this lesion.
4. Recovery of AE associated with prior antitumor therapy to CTCAE ≤ Grade 1 (except for Grade 2 alopecia).
5. ECOG score ≤ 1 within 7 days prior to first dose of study drug.
6. expected survival ≥ 12 weeks.
7. Subjects with chronic HBV infection must have HBV-DNA \< 1000 copies/ml and must agree to receive antiviral therapy according to treatment guidelines for patients with hepatitis B surface antigen positivity; patients with HCV-RNA positivity must agree to receive antiviral therapy according to treatment guidelines and have liver function at CTCAE ≤ grade 1.
8. Normal major organ function, i.e., the following criteria are met (no transfusion, erythropoietin, or colony-stimulating factor (G-CSF)…