IN10018 Combination Therapy in Previously-treated Solid Tumors

A Multicenter, Open-Label, Randomized, Phase Ib/II Clinical Trial to Evaluate the Efficacy, Safety, Tolerability, and Pharmacokinetics of IN10018 Combined With Taxane and Anti-PD-1/L1 Monoclonal Antibody in Previously-treated Solid Tumors

This is a phase Ib/II, randomized, open-label, multicenter clinical trial to evaluate the antitumor activities, safety, tolerability and pharmacokinetics (PK) of IN10018 in combination with taxane and anti-PD-1/L1 monoclonal antibody in patients with locally advanced or metastatic solid tumors who have failed in or been intolerant to at least one line of standard therapy. This study will be firstly carried out in previously-treated non-small cell lung cancer (NSCLC) population,

Study Overview

• Status: Withdrawn
• Conditions: Solid Tumor
• Intervention / Treatment: Drug: IN10018; Drug: Nab-paclitaxel; Drug: Tislelizumab

Detailed Description

This study consists of 2 parts: 1) Phase Ib-Dose Confirmation part: To assess the safety and recommended phase II dose (RP2D) of IN10018 in combination with taxane (nab-paclitaxel is proposed) and anti-PD-1/L1 monoclonal antibody (Tislelizumab is proposed) in previously-treated solid tumors. 2) Phase II-Dose Expansion part: To assess the antitumor efficacy and safety of IN10018+nab-paclitaxel+Tislelizumab as compared to nab-paclitaxel+Tislelizumab in previously-treated solid tumors. This study will be firstly carried out in previously-treated NSCLC population, and after getting enough efficacy and safety data of IN10018+nab-paclitaxel+Tislelizumab in NSCLC population and also taken into consideration of disease background of other specific solid tumors, sponsor will decide if to expand the treatment regimen into other solid tumors.

• Study Type: Interventional
• Phase: Phase 2; Phase 1

Contacts and Locations

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

1. Male or female aged 18-75 years old at the time of signing informed consent.
2. Be able to understand and be willing to sign informed consent.

3. Histologically or cytologically confirmed NSCLC, which is not suitable for locallly radical therapy.

   Note: Subjects should have received prior platinum-based doublet chemotherapy and anti-PD-1/L1-based systemic therapy and failed in treatment.

4. Subjects who have failed in 1- to 2 prior lines of standard systemic therapy.
5. Has at least one measurable tumor lesion per RECIST 1.1.
6. Has an ECOG performance status of 0 or 1.
7. Estimated life expectancy is more than 3 months.
8. Has adequate organ function.
9. AEs due to prior antitumor therapy must be recovered to ≤ Grade 1 (CTCAE v5.0) or a steady state as assessed by investigators
10. Subjects (male and female) with childbearing potential must agree to use contraception during the treatment phase and through 3 months after the last dose of study treatment.

Exclusion Criteria:

1. Previously documented EGFR, ALK and ROS1 mutation.
2. Have received chemotherapy, biological therapy, endocrine therapy, immunotherapy and other antitumor drugs within 4 weeks prior to the first dose of study treatment.
3. Have received other antitumor investigational drugs or treatments within 4 weeks prior to the first dose of study treatment.
4. Have received radiotherapy within 14 days prior to the first dose of study treatment.
5. Have had allogeneic haematopoietic stem cell transplantation or organ transplantation.
6. History of autoimmune disease within the past 2 years.
7. Have an immunodeficiency disorder or have received systemic steroid therapy (prednisone or equivalent corticosteroid > 10 mg/day) or other immunosuppressants within 7 days prior to the first dose of study treatment.
8. Currently have interstitial pneumonitis.
9. Have had FAK inhibitors treatment.
10. Have received prior nab-paclitaxel treatment and the first documented disease progression/recurrence is within 6 months since the last dose of nab-paclitaxel treatment.
11. Malignancies other than the study disease within 3 years prior to the first dose of study treatment.
12. Active central nervous system (CNS) metastases and/or carcinogenic meningitis.
13. Has a history of severe cardiovascular or cerebrovascular diseases within 6 months prior to the first dose.
14. Pleural, pericardial or abdominal effusion that are clinically symptomatic and require puncture or drainage.
15. Any active infection requiring systemic therapy within 14 days prior to the first dose of study treatment.
16. Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the study. Note: Subjects who have experienced Grade ≥ 3 immuno-related AEs (irAEs) during prior immunotherapy will not be enrolled.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Experimental Group; IN10018 + nab-paclitaxel + Tislelizumab in previously-treated NSCLC	Drug: IN10018; orally taken once daily; Other Names: BI 853520; Drug: Nab-paclitaxel; 125 mg/m2 D1, 8 Q3W, Intravenously; Drug: Tislelizumab; 200mg Q3W, Intravenously
Active Comparator: Control Group; Nab-paclitaxel + Tislelizumab in previously-treated NSCLC	Drug: Nab-paclitaxel; 125 mg/m2 D1, 8 Q3W, Intravenously; Drug: Tislelizumab; 200mg Q3W, Intravenously

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Recommended phase II dose (RP2D) of IN10018 in combination with nab-paclitaxel and Tislelizumab	Evaluate the number of patients with dose-limited toxicities (DLTs); Determine the RP2D of IN10018 in combination with nab-paclitaxel and Tislelizumab.	3 years
Objective response rate (ORR) of IN10018+nab-paclitaxel+Tislelizumab as compared to nab-paclitaxel+Tislelizumab in previously-treated solid tumors per blinded independent central review (BICR) based on RECIST 1.1	Defined as the proportion of subjects with complete response (CR) or partial response (PR)	3 years

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Progression-free survival (PFS) of IN10018+nab-paclitaxel+Tislelizumab as compared to nab-paclitaxel+Tislelizumab in previously-treated solid tumors per BICR and investigators based on RECIST 1.1	Defined as the time from randomization to first documentation of disease progression or to death due to any cause, whichever comes first.	3 years
Duration of objective response (DOR) of IN10018+nab-paclitaxel+Tislelizumab as compared to nab-paclitaxel+Tislelizumab in previously-treated solid tumors per BICR and investigators based on RECIST 1.1	Defined as the time from start of the first documentation of CR or PR to the first documentation of disease progression or to death due to any cause, whichever comes first.	3 years
Disease Control Rate (DCR) of IN10018+nab-paclitaxel+Tislelizumab as compared to nab-paclitaxel+Tislelizumab in previously-treated solid tumors per BICR and investigators based on RECIST 1.1.	Defined as the proportion of patients with CR, PR, or stable disease (SD).	3 years
Objective response rate (ORR) of IN10018+nab-paclitaxel+Tislelizumab as compared to nab-paclitaxel+Tislelizumab in previously-treated solid tumors per investigators based on RECIST 1.1.	Defined as the proportion of subjects with complete response (CR) or partial response (PR).	3 years
Overall survival (OS) in IN10018+nab-paclitaxel+Tislelizumab as compared to nab-paclitaxel+Tislelizumab in previously-treated solid tumors.	Defined as the time from randomization to the date of death due to any cause.	3 years
Number of patients with adverse event	The number of participants who experienced AEs is presented.	3 years
PK: AUC of IN10018 following single dose administration and at steady state	Area under the concentration-time curve (AUC)	3 years
PK: Cmax of IN10018 following single dose administration and at steady state	Maximum concentration (Cmax)	3 years
PK:Ctrough of IN10018 following single dose administration and at steady state	Trough concentration (Ctrough)	3 years
PK:Tmax of IN10018 following single dose administration and at steady state	Time to Cmax (Tmax)	3 years
PK:t1/2 of IN10018 following single dose administration and at steady state	Elimination half-life (t1/2).	3 years
PK:CL/F of IN10018 following single dose administration and at steady state	apparent clearance (CL/F)	3 years
PK:Vd/F of IN10018 following single dose administration and at steady state	Apparent volume of distribution (Vd/F)	3 years

Collaborators and Investigators

• Sponsor: InxMed (Shanghai) Co., Ltd.
• Investigators: Principal Investigator: Jifeng Feng, Jiangsu Province Cancer Hosipital

Study record dates

Study Major Dates

• Study Start (Estimated): August 13, 2025
• Primary Completion (Estimated): December 31, 2026
• Study Completion (Estimated): December 31, 2026

Study Registration Dates

• First Submitted: July 13, 2023
• First Submitted That Met QC Criteria: August 1, 2023
• First Posted (Actual): August 8, 2023

Study Record Updates

• Last Update Posted (Actual): March 27, 2026
• Last Update Submitted That Met QC Criteria: March 23, 2026
• Last Verified: April 1, 2025

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Neoplasms; Antineoplastic Agents, Immunological; Antineoplastic Agents; Molecular Mechanisms of Pharmacological Action; Tubulin Modulators; Antimitotic Agents; Mitosis Modulators; Antineoplastic Agents, Phytogenic; 130-nm albumin-bound paclitaxel; tislelizumab
• Other Study ID Numbers: IN10018-017

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No