A Study of RC118 in Patients With Locally Advanced Unresectable/Metastatic Solid Tumours

NCT04914117 | Completed Phase 1

• 1 other identifier: RC118G001
• Study Type: interventional
• Target: 7
• Locations: 1 country
• Sites: 4

Brief Summary

This is a Phase 1, First-in-Human, Multicentre, Open-label Study of RC118 for Injection in Patients with Locally Advanced Unresectable/Metastatic Solid Tumours to determine the safety and tolerability of RC118, including the maximum tolerated dose (MTD)/maximum administered dose (MAD), and to define the recommended Phase II dose (RP2D).

Conditions

Unresectable Solid Tumor; Metastatic Solid Tumor; Locally Advanced Solid Tumor

Outcome Measures

Primary Outcomes (3)

• MTD/MAD based on number of dose-limiting toxicities (DLTs)

  The maximum tolerated dose (MTD)/maximum administered dose (MAD) will be assessed based on the number of patients experiencing DLTs, graded according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) v5.0. If the MTD cannot be reached in this study, the MAD will be recorded.

  Up to 18 months

• Determine Recommended Phase 2 Dose (RP2D)

  The RP2D may be selected based on the MTD/MAD following consultation with the safety monitoring committee with all available data.

  Up to 18 months

• Adverse Events

  The adverse events occurring or worsening on or after the first dose of the study drug will be recorded.

  Up to 18 months

Secondary Outcomes (8)

• Object Response Rate (ORR)

  Up to 18 months

• Progression Free Survival (PFS)

  Up to 18 months

• Disease Control Rate (DCR)

  Up to 18 months

• Duration of response (DOR)

  Up to 18 months

• Immunogenicity

  Up to 18 months

Other Outcomes (1)

• CLDN18.2 expression

  Up to 18 months

Study Arms (1)

RC118 for injection

EXPERIMENTAL

Part A (Dose Escalation): RC118 will be administered through IV infusion at the various dose levels, including 0.25, 0.5, 1.0, 1.5, 2, 2.5, and 3 mg/kg, 1-12 subjects for each dose level. Part B (Dose Confirmation): RC118 will be administered at up to two dose levels, which is equal or lower than MTD/MAD, through IV infusion. Each dose level contains 3-6 subjects.

Drug: RC118 for injection

Interventions

RC118 for injection DRUG

RC118 will be administered intravenously (IV) on Day 1 of every 14-day cycle.

RC118 for injection

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Patients must be able to provide documented voluntary informed consent.
• Male or female patient ≥ 18 years and ≤ 75 years.
• Eastern Cooperative Oncology Group (ECOG) performance status (PS) score 0 or 1.
• The expected survival period exceeds 12 weeks.
• At least one target lesion that can be measured per Response Evaluation Criteria in Solid Tumours (RECIST) v1.1.
• Histologically documented, incurable, unresectable locally advanced or metastatic tumours that are intolerable or refractory to standard therapies.
• Patients agree to provide pre-treatment archived /biopsy tumour samples for retrospective Claudin 18.2 test. Archival tumour tissue should be from the most recent timepoint before entering the trial. In addition, archived samples obtained out of the screening are acceptable if it is discussed and approved by the Investigator and Sponsor in advance. Only when archived samples cannot be obtained, the biopsy will be considered at screening. Fresh tumour biopsies will NOT be considered if significant risk procedures are required with the discretion of Investigator.
• Adequate bone marrow, liver, and renal function defined as: absolute neutrophil count (ANC) ≥ 1.5 × 109/L, platelet ≥ 100 × 109/L, haemoglobin ≥ 90 g/L, serum total bilirubin ≤ 1.5 × upper limit of normal (ULN), ALT, AST or ALP ≤ 2.5 × ULN (≤ 5 × ULN when there is known liver metastasis), serum creatinine ≤ 1.5 × ULN, INR ≤ 1.5 × ULN, APTT ≤ 1.5 × ULN.
• Willingness to avoid pregnancy or fathering children based on the criteria below:
• Female patients of childbearing potential and male patients with partners of childbearing potential treated with RC118, must agree to use a highly effective form(s) of contraception during study and within 6 months after the last dose. Those methods include but not limited to combined (oestrogen and progestogen containing) hormonal contraception, intrauterine device, intrauterine hormone-releasing system, bilateral tubal occlusion or vasectomized partner (on the understanding that this is the only one partner during the whole study duration), and sexual abstinence.
• Females of non-childbearing potential (e.g., surgically sterile with a hysterectomy and/or bilateral oophorectomy or chemically sterile or ≥ 12 months of amenorrhea in the absence of chemotherapy, anti-oestrogens, or ovarian suppression). Those females do not need to undergo pregnancy test.

You may not qualify if:

• Women who are pregnant or breastfeeding.
• Diagnosed active hepatitis B infection (defined as positive of hepatitis B surface Ag and hepatitis B DNA≥500IU/ml), active hepatitis C infection (defined as presence of hepatitis C RNA), and human immunodeficiency virus infection (defined as positive HIV test) during the screening period.
• Received vaccines within 4 weeks prior to administration or plan on receiving any vaccine during the study.
• Subjects with a history of other acquired/congenital immunodeficiency diseases or organ transplantation.
• Patients have history of targeted therapy of Claudins, or participated in other clinical trials and received investigational product within 4 weeks before the first administration of study drug.
• Allergic constitution or allergic to known research drug active ingredients or excipient.
• Patients who are under the treatment of anticoagulant drugs (e.g., warfarin, apixaban, and heparin). Patients using prophylactic doses of heparin (e.g., LMWH) is eligible in the study.
• Patients undergoing any anti-tumour therapy, including surgery, chemotherapy, radiotherapy and biological therapy, within 4 weeks prior to the first administration of study drug, or palliative radiotherapy for bone/other solitary metastases within 2 weeks prior to the first administration of study drug.
• Previous adverse reactions resulting from previous anti-tumour therapies, which have not returned to Grade 0 or 1 according to NCI-CTCAE v5.0 (except alopecia) at screening.
• There are clinical symptoms of fluid in the third space (e.g., large amounts of pleural fluid or ascites) that cannot be controlled by drainage or other therapies.
• A clinically significant active infection judged by the investigator.
• Comorbidities that may seriously endanger the patient's safety or affect the completion of the study, such as gastrointestinal bleeding (within 4 weeks prior to the screening period), peptic ulcer, intestinal obstruction, intestinal paralysis, interstitial pneumonia, pulmonary fibrosis, kidney failure, and uncontrolled diabetes.
• QTc interval \> 480 ms in both male and female (based on the mean value of the triplicate screening ECGs); family or personal history of long/short QT syndrome, History of ventricular arrhythmia deemed clinically significant by the investigator, or currently receiving antiarrhythmic drug treatment, or implantation of arrhythmia defibrillation device.
• History of myocardial infarction within 6 months prior to the screening period, severe or unstable angina pectoris, coronary or peripheral artery bypass grafting, heart failure ≥ 3 (New York Heart Association), or uncontrolled hypertension.
• Patients with known current alcohol dependence or drug abuse.

Sponsors & Collaborators

• RemeGen Co., Ltd.: lead

Study Sites (4)

Remegen Site #12

Macquarie Park, New South Wales, 2109, Australia

Location

Remegen Site #14

Bedford Park, South Australia, 5042, Australia

Location

Remegen Site #13

Frankston, Victoria, 3199, Australia

Location

Remegen Site #11

Malvern, Victoria, 3144, Australia

Location

MeSH Terms

Conditions

Neoplasm Metastasis

Interventions

Injections

Condition Hierarchy (Ancestors)

Neoplastic Processes; Neoplasms; Pathologic Processes; Pathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Drug Administration Routes; Drug Therapy; Therapeutics

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: May 21, 2021
• First Posted: June 4, 2021
• Study Start: November 29, 2021
• Primary Completion: November 15, 2022
• Study Completion: March 11, 2023
• Last Updated: June 22, 2023

Record last verified: 2023-06

Data Sharing

• IPD Sharing: Will not share

Locations

AU (4)