A Study of AK112 Monotherapy in Advanced/Metastatic Renal Cell Carcinoma
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: AK112 monotherapy.
- Who it may be relevant to
- Registry conditions: Renal Cell Carcinoma. Basic parameters: 18 years — 75 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
This is an open-label, single arm , Ib/II phase trial to evaluate the efficacy and safety of AK112（ivonescimab）monotherapy as first-line treatment for favourable risk advanced/metastatic renal cell carcinoma (a/m RCC). Subjects will receive AK112 until disease progression, unacceptable toxic effects, death，a decision by the physician or patient to withdraw from the trial，or AK112 exposure over 2 years. The study set dose exploration stage and dose expansion stage respectively. Firstly, include a few subjects for observation in dose exploration stage, and select appropriate dose to enter expansion, then continue to include more subjects to further assessment.
Interventions
- Drug AK112 monotherapy
A novel PD-1/VEGF bispecific antibody; RP2D intravenously (IV)，Q3W
Primary outcome measures
- ORR per RECIST v1.1 assessed by investigators [Time frame: Up to 2 years]
Secondary outcome measures (5)
- DCR per RECIST v1.1 as assessed by investigators [Time frame: Up to 2 years]
- Duration of response (DOR) [Time frame: Up to 2 years]
- Progression-free survival (PFS) [Time frame: 3 years]
- Overall survival (OS) [Time frame: 4 years]
- Treatment-related adverse events [Time frame: 3 years]
Eligibility criteria
Inclusion criteria
- Provide written informed consent/assent for the trial.
- Be ≥18 and ≤ 75 years of age on day of signing informed consent, no matter male or female.
- IMDC favourable risk（IMDC score 0）.
- ECOG PS 0-1.
- Have estimated life expectancy of at least 3 months.
- Have histologically or cytologically confirmed diagnosis of RCC with mainly clear cell carcinoma component.
- Have received no prior systemic therapy for advanced RCC，Including but not limited to Immunotherapy, target therapy, chemotherapy, biological therapy, etc.
Note: Prior neoadjuvant/adjuvant therapies are acceptable if disease progression occurred > 6 months after last dosage of neoadjuvant/adjuvant treatment.
- Have measurable disease per RECIST v1.1 .
- Adequate organ function.
- Contraception from entering the trial，until 120 days after the last administration of the investigational drug.
- Willing to comply with the scheduled visits, treatment plans, and other requirements of the trial.
Exclusion criteria
- non-clear cell renal cell carcinoma，nccRCC（e.g. chromophobe, papillary)
- Has active autoimmune disease that might deteriorate when receiving an immunostimulatory agents. Subjects with diabetes type I, vitiligo, psoriasis, hypo-or hyperthyroid disease not requiring immunosuppressive treatment are eligible.
- Has a known additional malignancy that has progressed or has required active treatment in the last 5 years.
Note: Subjects with basal cell carcinoma of the skin, squamous cell carcinoma of the skin that has undergone potentially curative therapy or carcinoma in situ are not excluded.
- Eligible for surgery.
- History of severe bleeding or coagulation disorders.
- History of abdominal fistula or gastrointestinal perforation related to anti VEGF therapy.
- Has previously received systemic therapy.
- Has newly diagnosed brain metastases or known symptomatic brain metastases requiring steroids.
- Had major surgery 4 weeks prior to receiving first dose of trial treatment.
- Has a diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other form of immunosuppressive therapy within 14 days prior to receiving first dose of trial treatment.
- Has an active tuberculosis and syphilitic infection.
- Has a known history of Human Immunodeficiency Virus (HIV) infection (HIV antibodies).
- Has known active Hepatitis B (e.g., Hepatitis B surface antigen \[HBsAg\] reactive and HBV-DNA>2000 IU/ml) or Hepatitis C virus (e.g., HCV RNA \[qualitative\] is detected).
- Has been pregnant or breastfeeding.
- Assessed by the investigator to be unable or unwilling to comply with the requirements of the protocol.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06472895 · AK112-001-II-RCC