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A Study of IBI363 in Subjects With Advanced Melanoma

Primary Purpose

Melanoma

Status
Not yet recruiting
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
IBI363
Sponsored by
Innovent Biologics (Suzhou) Co. Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Melanoma

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Histologically and/or cytologically confirmed, unresectable, locally advanced or metastatic melanoma (according to the American Joint Committee on Cancer (AJCC) 8th edition staging III-IV). Progression or recurrence after at least first-line systemic standard treatment. At least one measurable lesion (target lesion) per RECIST v1.1. Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0 or 1. Life expectancy of 3 months or more. Female subjects of childbearing age or male subjects whose partners are female subjects of childbearing age agree to strictly adopt effective contraceptive measures throughout the entire treatment period and 6 months after the treatment period. Exclusion Criteria: Pregnant or lactating subjects, or subjects who plan to conceive before, during, or within 6 months after the last dose of the study drug. Active or symptomatic central nervous system metastasis. At baseline (within 7 days before the first administration of the study drug), there were any hematological abnormalities as follows: hemoglobin<90 g/L; Absolute neutrophil count (ANC)<1.5 × 109/L; Platelet count<100 × 109/L. At baseline (within 7 days prior to first administration), there were any serum biochemical abnormalities as follows: Total bilirubin>1.5 × ULN; AST or ALT>3 × ULN; If it is tumor liver metastasis, AST or ALT>5.0 × ULN; Serum creatinine>1.5 × ULN or CCr<45 mL/min, using the Cockcroft Fault formula to calculate CCr (using actual body weight); Albumin<30 g/L. At baseline (within 7 days before first administration), there were any coagulation parameter abnormalities as follows: INR>1.5 × ULN (>3 if receiving anticoagulant therapy with stabilizer dosage) × ULN); PTT (or activated partial thromboplastin time (aPTT))>1.5 × ULN (>3 if receiving anticoagulant therapy with stabilizer dosage) × ULN). History of active thrombosis, deep vein thrombosis, or pulmonary embolism within 4 weeks prior to the first administration of the investigational drug, unless sufficient treatment has been given and the investigator believes that the condition is stable. Uncontrolled bleeding or known tendency to bleed.

Sites / Locations

  • Beijing Cancer Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

IBI363

Arm Description

Outcomes

Primary Outcome Measures

Phase Ⅰb: AE(Adverse event)
Phase Ⅰb: RP2D(Recommended phase 2 dose)
Phase Ⅱ:ORR(Objective response rate)

Secondary Outcome Measures

DoR(duration of response)
PFS(progression free survival)
OS(overall survival)
DCR(disease control rate)
TTR(time to response)
TTP(time to progression)

Full Information

First Posted
October 7, 2023
Last Updated
October 7, 2023
Sponsor
Innovent Biologics (Suzhou) Co. Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT06081920
Brief Title
A Study of IBI363 in Subjects With Advanced Melanoma
Official Title
A Phase Ib/II Study to Evaluate the Safety, Tolerability, and Efficacy of IBI363 in Subjects With Advanced Melanoma
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 13, 2023 (Anticipated)
Primary Completion Date
June 6, 2025 (Anticipated)
Study Completion Date
July 31, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Innovent Biologics (Suzhou) Co. Ltd.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This is an open-label, multicenter Phase Ib/II study to evaluate the safety, tolerability, and efficacy of IBI363 in advanced melanoma patients

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Melanoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
IBI363
Arm Type
Experimental
Intervention Type
Biological
Intervention Name(s)
IBI363
Intervention Description
RP2D of IBI363
Primary Outcome Measure Information:
Title
Phase Ⅰb: AE(Adverse event)
Time Frame
2 year
Title
Phase Ⅰb: RP2D(Recommended phase 2 dose)
Time Frame
2 year
Title
Phase Ⅱ:ORR(Objective response rate)
Time Frame
2 year
Secondary Outcome Measure Information:
Title
DoR(duration of response)
Time Frame
2 year
Title
PFS(progression free survival)
Time Frame
2 year
Title
OS(overall survival)
Time Frame
2 year
Title
DCR(disease control rate)
Time Frame
2 year
Title
TTR(time to response)
Time Frame
2 year
Title
TTP(time to progression)
Time Frame
2 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically and/or cytologically confirmed, unresectable, locally advanced or metastatic melanoma (according to the American Joint Committee on Cancer (AJCC) 8th edition staging III-IV). Progression or recurrence after at least first-line systemic standard treatment. At least one measurable lesion (target lesion) per RECIST v1.1. Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0 or 1. Life expectancy of 3 months or more. Female subjects of childbearing age or male subjects whose partners are female subjects of childbearing age agree to strictly adopt effective contraceptive measures throughout the entire treatment period and 6 months after the treatment period. Exclusion Criteria: Pregnant or lactating subjects, or subjects who plan to conceive before, during, or within 6 months after the last dose of the study drug. Active or symptomatic central nervous system metastasis. At baseline (within 7 days before the first administration of the study drug), there were any hematological abnormalities as follows: hemoglobin<90 g/L; Absolute neutrophil count (ANC)<1.5 × 109/L; Platelet count<100 × 109/L. At baseline (within 7 days prior to first administration), there were any serum biochemical abnormalities as follows: Total bilirubin>1.5 × ULN; AST or ALT>3 × ULN; If it is tumor liver metastasis, AST or ALT>5.0 × ULN; Serum creatinine>1.5 × ULN or CCr<45 mL/min, using the Cockcroft Fault formula to calculate CCr (using actual body weight); Albumin<30 g/L. At baseline (within 7 days before first administration), there were any coagulation parameter abnormalities as follows: INR>1.5 × ULN (>3 if receiving anticoagulant therapy with stabilizer dosage) × ULN); PTT (or activated partial thromboplastin time (aPTT))>1.5 × ULN (>3 if receiving anticoagulant therapy with stabilizer dosage) × ULN). History of active thrombosis, deep vein thrombosis, or pulmonary embolism within 4 weeks prior to the first administration of the investigational drug, unless sufficient treatment has been given and the investigator believes that the condition is stable. Uncontrolled bleeding or known tendency to bleed.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xiu'zhi Yu
Phone
0512-69566088
Email
xiuzhi.yu@innoventbio.com
Facility Information:
Facility Name
Beijing Cancer Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100142
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jun Guo
Phone
13911233048
Email
guoj307@126.com

12. IPD Sharing Statement

Plan to Share IPD
No

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A Study of IBI363 in Subjects With Advanced Melanoma

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