Evaluation of JSKN016 Combination Therapy in Subjects With NSCLC
- Summary
- This is a Phase Ib clinical study conducted in China to evaluate the treatment of advanced non-small cell lung cancer with JSKN016 in combination therapy. The enrolled subjects are all in the locally advanced or metastatic stage of non-small cell lung cancer.
- Short title
- Evaluation of JSKN016 Combination Therapy in Subjects With NSCLC
- Official title
- Evaluation of JSKN016 Combination Therapy in Subjects With Advanced Non-Small Cell Lung Cancer: A Phase Ib Study
- Control arm
- Open label
- Registry reports results
- Listing at source
- Listed
- Recruitment status
- Recruiting
- Phase
- Phase 1
- Study type
- Interventional
- Completion date
- 2028-12-30
- First posted
- 2025-03-11
- Registry last updated
- 2026-03-30
- Primary completion date
- 2028-06-30
- Start date
- 2025-04-02
- Participants
- Participant count basis
- Estimated
- Planned participants
- Protocol amendments
- Number of sites
- Data monitoring committee
- Registry sponsor category
- Industry
- Lead sponsor
- Jiangsu Alphamab Biopharmaceuticals Co., Ltd
- Source registry
- ClinicalTrials.gov
- Registry ID
- NCT06868732
- ClinicalTrials.gov ID
- NCT06868732
- Registry record
- Open registry record
- Allocation
- Not randomised
- Model
- Parallel groups
- Purpose
- Treatment
- Masking
- No masking
ORR assessed by the investigator per RECIST v1.1
Timeframe: Up to 24months
Objective response rate (ORR) was defined as the proportion of participants who achieve either complete response \[CR\] or partial response \[PR\] per Response Evaluation Criteria in Solid Tumors (RECIST v1.1)
Safety reflected by AE
Timeframe: Up to 24months
An AE is any untoward medical occurrence in a participant, temporally associated with the use of study treatment, whether or not considered related to the study treatment.
DOR assessed by the investigator per RECIST v1.1
Timeframe: Up to 24months
Duration of response (DoR) assessed according to RECIST v1.1.
DCR assessed by the investigator per RECIST v1.1
Timeframe: Up to 24months
Disease control rate (DCR) assessed according to RECIST v1.1.
TTR assessed by the investigator per RECIST v1.1
Timeframe: Up to 24months
Time to response (TTR) is defined as the time to response base on RECIST v1.1.
PFS assessed by investigator per RECIST v1.1
Timeframe: Up to 24months
Progression-free survival (PFS) is defined as the time from the date of initial administration till the first documentation of disease progression assessed by the investigator or death due to any cause (whichever occurs first).
OS
Timeframe: Up to 24months
Overall Survival (OS) is defined as the time from the date of initial administration till death due to any cause.
Peak Plasma Concentration (Cmax)
Timeframe: Up to 24months
The Peak Plasma Concentration (Cmax) of the antibody-drug conjugate (ADC), total antibody and free payload.
Trough Plasma Concentration (Cmin)
Timeframe: Up to 24 months
The Trough Plasma Concentration (Cmin) of the antibody-drug conjugate (ADC), total antibody and free payload.
ADA
Timeframe: Up to 24months
Number of subjects with detectable anti-drug antibodies (ADA).
- Sex
- All
- Age groups
- Adults, Older adults
- Minimum age
- 18 Years
- Maximum age
- 75 Years
- Healthy volunteers
- No
- Voluntarily participate and sign the informed consent form.
- Age ≥ 18 years old, ≤ 75 years old, male or female.
- Eastern Cooperative Oncology Group performance status (ECOG PS) score of 0 or 1.
- Expected survival ≥ 3 months.
- Histologically or cytologically confirmed locally advanced or metastatic non-small cell lung cancer (NSCLC) that is not suitable for radical surgery and/or radical radiotherapy.
- At least one extracranial measurable lesion at baseline according to RECIST 1.1 criteria.
- Recently archived or fresh tumor tissue samples are available.
- Have good organ function.
- Have no current birth plans and agree to contraception during the trial.
- Presence of any small cell carcinoma component in histopathology.
- Subjects with other malignant tumors within 5 years prior to enrollment, and other tumors have been cured through local therapy, such as cured cutaneous squamous cell carcinoma, basal cell carcinoma, non-primary invasive bladder cancer, and prostate/cervical/breast cancer in situ.
- Presence of brainstem, meningeal metastases, spinal cord metastases or compression, leptomeningeal metastases, or history of carcinomatous meningitis; Presence of active brain metastases.
- During the screening period, imaging shows that the tumor invades, compresses, or occurs in the surrounding important organs (such as the heart and pericardium, trachea, esophagus, superior vena cava, etc.) or there is a risk of esophageal tracheal fistula or esophageal pleural fistula.
- Adequate washout of previous therapy before the first dose.
- Gastrointestinal abnormalities with obvious clinical manifestations.
- Presence of clinically severe respiratory impairment caused by pulmonary disease complications.
- Presence of cardiovascular and cerebrovascular diseases or cardiovascular and cerebrovascular risk factors.
- Prior treatment with topoisomerase I inhibitors (e.g., irinotecan, topotecan), antibody-drug conjugates containing topoisomerase I inhibitors (e.g., DS-8201, HER3-DXd, DS-1062), or targeting TROP2 or HER3.
- Previous treatment with docetaxel.
- Have an uncontrolled infection, a history of immunodeficiency, a positive human immunodeficiency virus (HIV) test, or a history of AIDS.
- Previous history of allogeneic bone marrow or organ transplantation.
- Known allergy to any component of the study drug, and previous history of severe allergic reaction to other antibody drugs.
- Pregnant and/or lactating females.
- Have local or systemic diseases caused by non-malignant tumors, or diseases or symptoms secondary to tumors, which can lead to higher medical risk and/or uncertainty in survival evaluation, such as tumor leukemia response , cachexia manifestations, etc.
- Sun Yat-sen University Cancer CenterGuangzhou, ChinaRecruiting
Related records
Drugs (6)
Lead sponsors (1)
Conditions (1)
- Non-small cell lung carcinoma Primary condition