3D011-08 Monotherapy in Subjects With Advanced Solid Tumors
- Registration Number
- NCT05099536
- Lead Sponsor
- 3D Medicines (Beijing) Co., Ltd.
- Brief Summary
The purpose of this study is evaluate the the safety, tolerability, pharmacokinetics profiles, and preliminary efficacy of 3D011-08 in subjects with advanced solid tumors.
- Detailed Description
Detailed Description: This study was initiated on February 24, 2022, at Fudan Cancer Hospital. However, noparticipants were screened or enrolled after the initiation. Due to strategic development adjustments, thecompany terminated the study on September 11. 2023.
Recruitment & Eligibility
- Status
- WITHDRAWN
- Sex
- All
- Target Recruitment
- Not specified
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Histologically or cytologically confirmed locally advanced or metastatic malignant solid tumors(part 1 dose escalation); Histologically confirmed locally advanced or metastatic hepatocellular carcinoma (cohort 1),advanced renal cell carcinoma (cohort 2), and metastatic castration-resistant prostate cancer (cohort 3) for which not amenable to local therapy.(part 2 dose expansion).
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Cohort 1 and 2: at least one measurable lesion (according to RECIST 1.1 criteria);Cohort 3: at least one measurable or unmeasurable lesion (according to RECIST 1.1 criteria).
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Subjects must have failed or have been intolerant to established standard therapies, or standard therapies did not exist or were no longer effective for a given tumor type, or in the opinion of the Investigator have been considered ineligible for a particular form of standard therapy on medical grounds(part 1 dose escalation). Cohort 1 (advanced hepatocellular carcinoma)and Cohort 2 (advanced renal cell carcinoma): Subjects had disease progression after received previous first-line of systemic treatment, or subjects are intolerant of or have refused to receive first-line of systemic treatment.
Cohort 3 (metastatic castration-resistant prostate cancer) : Patients who had failed or had refused prior abiraterone and/or docetaxel chemotherapy.(part 2 dose expansion)
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ECOG Performance Status ≤ 2(part 1 dose escalation).≤ 1.(part 2 dose expansion)
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Life expectancy ≥ 12 weeks.
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Adequate organ and bone marrow function.
- Investigational products or devices in other clinical trials or received antibody drug therapy within 4 weeks before the first dose,or chemotherapy, targeted therapies,or radiotherapy within 2 weeks before the first dose.
- Participants need to continue using medications known to have a significant risk of causing QTc prolongation or a CYP3A4 strong inhibitor or strong inducer.
- Participants who have previous toxicity of anti-tumor therapy that has not been returned to level 0 or 1.
- Participants with diseases at risk of bleeding within 3 months prior to enrollment
- Participants with concomitant medical conditions requiring anticoagulant therapy at a therapeutic dose
- History or current condition of uncontrolled cardiovascular disease.
- Participants with gastrointestinal disease associated with a risk of perforation or fistula formation
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SEQUENTIAL
- Arm && Interventions
Group Intervention Description 3D011-08 3D011-08 -
- Primary Outcome Measures
Name Time Method ORR 24 Months proportion of subjects in cohort 1 and cohort 2 who achieved a confirmed complete response (CR) or partial response (PR) based on RECIST v1.1 as assessed by investigators.
TTP 24 Months time to progression based on the PCWG3 recommendations for assessment of prostate cancer disease progression (CT/MRI, bone scan) as assessed by investigators .
Maximum Tolerated Dose (MTD) of3D011-08 24 months The maximum tolerated dose as determined in Part 1 of the study will be used as the recommended dose for Part 2.
- Secondary Outcome Measures
Name Time Method Tmax 24 months AUC0~t、AUC0~∞ 24 months Ctrough 24 months t1/2 24 months CL 24 months Vd 24 months ORR 24 months proportion of subjects in part of Dose Escalation who achieved a confirmed complete response (CR) or partial response (PR) based on RECIST v1.1 as assessed by investigators.proportion of subjects in dose expansion cohort 3 who achieved a confirmed complete response (CR) or partial response (PR) based on the PCWG3 recommendations for assessment of prostate cancer disease progression (CT/MRI, bone scan) as assessed by investigators .
Duration of response (DoR) 24 months DoR is defined as the time from the date of first CR or PR based on RECIST v1.1 to the date of first documented progressive disease based on RECIST v1.1 or death, whichever occurs first.part1 Dose Escalation，part 2 dose expansion:Cohort 1 and Cohort 2.
Disease control rate (DCR) 24 months defined as the proportion of subjects who achieve a confirmed complete response (CR) or partial response (PR) or stable disease (SD) based on RECIST v1.1 as assessed by investigators.Proportion of subjects in dose expansion cohort 3 who achieve a confirmed complete response (CR) or partial response (PR) or stable disease (SD) based on the PCWG3 recommendations for assessment of prostate cancer disease progression (CT/MRI, bone scan) as assessed by investigators .
Progression-free survival (PFS) 24 months PFS is defined as the time from the date of first study dose to disease progression based on RECIST v1.1 or death, whichever occurs first. Subjects in dose expansion cohort 3 based on the PCWG3 recommendations for assessment of prostate cancer disease progression (CT/MRI, bone scan) as assessed by investigators .
Permeable surface area of capillary wall(PS) 24 months RPTD 24 months RP2D will be determined based on pharmacodynamics or clinical response, as well as the incidence rate and nature of the toxicities observed.
Incidence and severity of adverse events (AEs) and serious adverse events (SAEs) 24 months Cmax Cmax 24 months Css min 24 months the incremental Area Under Curve (iAUC) 24 months
Trial Locations
- Locations (1)
Fudan University Shanghai Cancer Center
🇨🇳Shanghai, Floor 2, Building 2, 270 Dong 'an Road, Xuhui District, China