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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT05867303




Registration number
NCT05867303
Ethics application status
Date submitted
17/04/2023
Date registered
19/05/2023
Date last updated
16/08/2024

Titles & IDs
Public title
A RC198 Study in Subjects With Locally Advanced Unresectable or Metastatic Solid Tumors
Scientific title
A Phase 1, First-in-Human, Multicenter, Open-Label Study to Evaluate the Safety, Tolerability, Pharmacokinetic, Immunogenetic and Efficacy of RC198 in Subjects With Locally Advanced Unresectable or Metastatic Solid Tumors
Secondary ID [1] 0 0
RC198-G001
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Melanoma 0 0
Urothelial Carcinoma 0 0
Renal Cell Carcinoma 0 0
Non-small Cell Lung Cancer 0 0
Head and Neck Squamous Cell Carcinoma 0 0
Colorectal Carcinoma 0 0
Condition category
Condition code
Cancer 0 0 0 0
Non melanoma skin cancer
Cancer 0 0 0 0
Kidney
Cancer 0 0 0 0
Head and neck
Cancer 0 0 0 0
Bowel - Back passage (rectum) or large bowel (colon)

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - RC198 Injection

Experimental: RC198 Injection - RC198 injection will be administered subcutaneously on Day 1 of Week 1 to Week 4 (inclusive) of each 6-week (42-day) cycle.


Treatment: Drugs: RC198 Injection
RC198 injection will be administered subcutaneously on Day 1 of Week 1 to Week 4 (inclusive) of each 6-week (42-day) cycle.
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
MTD based on number of dose-limiting toxicities (DLTs)
Timepoint [1] 0 0
First 4 weeks (28 days) after first dose of study drug
Primary outcome [2] 0 0
Determine Recommended Phase 2 Dose (RP2D)
Timepoint [2] 0 0
Informed consent through 28 days after the last dose of study drug
Primary outcome [3] 0 0
Incidence of Adverse Events [Safety and tolerability]
Timepoint [3] 0 0
Informed consent through 28 days after the last dose of study drug
Secondary outcome [1] 0 0
Time to maximum serum concentration [Tmax]
Timepoint [1] 0 0
Day 1- Day 5 of Week 1 and Week 4, Day 1 of Week 2, Week 3, Week 5 and Week 6 during cycle 1, and Day 1 of Week 1 and Week 4 during subsequent cycles, and EOT (7 days within subject discontinued study drug)
Secondary outcome [2] 0 0
Area under the serum concentration verus time curve [AUC]
Timepoint [2] 0 0
Day 1- Day 5 of Week 1 and Week 4, Day 1 of Week 2, Week 3, Week 5 and Week 6 during cycle 1, and Day 1 of Week 1 and Week 4 during subsequent cycles, and EOT (7 days within subject discontinued study drug)
Secondary outcome [3] 0 0
Maximum serum Concentration [Cmax]
Timepoint [3] 0 0
Day 1- Day 5 of Week 1 and Week 4, Day 1 of Week 2, Week 3, Week 5 and Week 6 during cycle 1, and Day 1 of Week 1 and Week 4 during subsequent cycles, and EOT (7 days within subject discontinued study drug)
Secondary outcome [4] 0 0
Immunogenicity of RC198
Timepoint [4] 0 0
D1 of W1 and W3 during cycle 1, and D1 of W1 during subsequent cycles, and EOT (7 days within subject discontinued study drug)
Secondary outcome [5] 0 0
Object Response Rate (ORR)
Timepoint [5] 0 0
Screening, then every 6 weeks (±7 days) after Day 1 of Cycle 1 Week 1 until 14 days after the last dose of the study drug. Assessed up to 24 months.
Secondary outcome [6] 0 0
Disease Control Rate (DCR)
Timepoint [6] 0 0
Screening, then every 6 weeks (±7 days) after Day 1 of Cycle 1 Week 1 until 14 days after the last dose of the study drug. Assessed up to 24 months.
Secondary outcome [7] 0 0
Duration of response (DoR)
Timepoint [7] 0 0
From first partial response (PR) or complete response (CR) until disease progression or death, whichever occurs first. Assessed up to 24 months.
Secondary outcome [8] 0 0
Progression Free Survival (PFS)
Timepoint [8] 0 0
From the first dose until documented disease progression or death, whichever occurs first. Assessed up to 24 months.

Eligibility
Key inclusion criteria
1. Subjects with the ability to understand and give written informed consent for participation in this trial, including all evaluations and procedures as specified by this protocol.
2. Subjects with locally advanced unresectable or metastatic solid tumors who experience disease progression after standard treatment, or unable to tolerate standard treatment, or refuse standard treatment.
3. At least 1 measurable or evaluable lesion per Response Evaluation Criteria In Solid Tumors (RECIST) v1.1.
4. Male or female aged = 18 years.
5. ECOG PS score of 0 or 1.
6. Anticipated life expectancy of > 12 weeks.
7. Adequate bone marrow, liver, and renal function defined as:

* Absolute neutrophil count = 1.5× 109/L.
* Absolute lymphocyte count = 500/µL.
* Platelet = 100 × 109/L.
* Hemoglobin = 90 g/L without receiving erythropoietin (EPO), granulocyte colony stimulating factor (G-CSF), or granulocyte-macrophage colony stimulating factor (GM-CSF) within 14 days and blood transfusion including red blood cell and platelet transfusion in at least 7 days prior to first dose of investigational product.
* Total bilirubin = 1.5 × ULN or up to 3 × ULN if Gilbert syndrome.
* Alanine aminotransaminase (ALT), aspartate aminotransferase (AST) = 2.5 × ULN when there is no liver metastasis. ALT, AST = 5 × ULN when there is liver metastasis
* Serum creatinine = 1.5 × ULN, or creatinine clearance = 60 mL/min (using Cockcroft-Gault formula); Urine protein < 2 + or 24 hour total urine protein quantity < 1g.
* Activated partial thromboplastin time (APTT) = 1.5× ULN; international normalized ratio (INR) = 1.5.
8. Left ventricular ejection fraction = 50%, as determined by echocardiogram or multiple-gated acquisition (MUGA) scan.
9. Willingness to avoid pregnancy or fathering children based on the criteria below:

1. Women of childbearing potential (WOCBP) who engage in heterosexual intercourse or male subjects whose sexual partners are WOCBP must be able to and agree to use an acceptable, highly effective, double barrier contraception commencing from Screening, during study, and for 6 months after the last dose of investigational product, including:

* Simultaneous use of hormonal contraceptives and must agree to use the same hormonal contraceptive throughout the study, and a condom for the male partner.
* Simultaneous use of intrauterine device (IUD) and condom for the male partner.
* Simultaneous use of diaphragm or cervical cap and condom for the male partner.
* Sterile male partner (vasectomized for at least 6 months prior to first dose of investigational product).
* True abstinence, defined as no sexual intercourse (heterosexual couples). Periodic abstinence and withdrawal are not acceptable methods.

Subjects with same-sex partners (abstinence from penile-vaginal intercourse) or who are abstinent from heterosexual intercourse are not required use contraception when this is their preferred and usual lifestyle.
2. WOCBP must have a negative serum beta human-chorionic gonadotropin (ß-hCG) pregnancy test at Screening and a negative pregnancy test on Day 1 of each cycle. In the event of a positive urine pregnancy test, a serum pregnancy test will be performed for confirmation.
3. Must agree not to donate ova or sperm from Screening, during study, and for 6 months after the last dose of investigational product
4. Must agree not to donate ova or sperm from Screening, during study, and for 6 months after the last dose of investigational product
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
1. Pregnant or lactating.
2. Known to be human immunodeficiency virus (HIV) positive, with active hepatitis (HBV) characterized by elevated levels of HBV ribonucleic acid exceeding the ULN; or active hepatitis C (HCV) with positive HCV ribonucleic acid (RNA); Subjects who are Hepatitis B surface antigen positive or hepatitis B core antibody positive must have undetectable quantitative DNA polymerase chain reaction (PCR).
3. Administration of a live vaccine within 28 days before first dose of investigational and during the study. Note: Seasonal vaccines for influenza or Coronavirus Disease 2019 (COVID-19) vaccines are generally inactivated vaccines and are allowed. Intranasal vaccines are live vaccines and are not allowed.
4. Previous anti-tumor therapies (including surgery, chemotherapy, traditional Chinese medicine, radiotherapy, immunotherapy, biological therapy, hormonal therapy, or investigational agents for cancer treatment) within 4 weeks or within 5 half-lives of anti-tumor agents, whichever is shorter, prior to the first dose of investigational product, or palliative radiotherapy for bone metastases within 2 weeks prior to the first dose of investigational product.
5. Previous adverse reactions resulting from previous anti-tumor therapies, which have not resolved to Grade 0 or 1 according to NCI CTCAE v5.0 (except for alopecia, fatigue, pigmentation and other conditions with no safety risk according to Investigator's opinion) or Baseline within 4 weeks prior to first administration of the investigational product.
6. Experienced prior Grade 3 or higher immune-related toxicity that resulted in permanent drug discontinuation (subjects with prior temporary drug interruptions due to endocrinopathies etc. are eligible).
7. History of therapy with an agent targeting of IL-15 or IL-2.
8. Known hypersensitivity to any excipient contained in the drug formulation of investigational products or supplements to be administered during the study.
9. Uncontrolled diseases including:

1. Uncontrolled infection requiring systematic antibiotics, antivirals or antifungals within 4 weeks prior to first administration of the investigational product.
2. Active infection with COVID-19.
3. Active tuberculosis infection, or still on anti-tuberculosis therapy or received anti-tuberculosis therapy within 1 year prior to first administration of the investigational product.
4. Symptomatic congestive heart failure Grade II-IV (New York Heart Association [NYHA]), symptomatic or uncontrolled arrhythmias, QTc interval > 480 ms or personal or family history of congenital long/short QT syndrome, Severe or unstable angina pectoris, coronary or peripheral artery bypass grafting.
5. Uncontrollable hypertension (systolic blood pressure = 160mmHg or diastolic blood pressure = 100mmHg).
6. Systemic diseases, including diabetes pulmonary fibrosis, acute lung disease, interstitial lung disease, cirrhosis, etc.
10. History of any arterial thromboembolic event within 6 months prior to the first administration of investigational product, including myocardial infarction, unstable angina pectoris, pulmonary embolism, cerebrovascular stroke, or transient ischemic attack, etc.
11. History of deep vein thrombosis or any other severe thromboembolism within 3 months prior to the first administration of investigational product (implantable venous access port or catheter-derived thrombosis, or superficial venous thrombosis is not considered as "severe" thromboembolism).
12. History of life-threatening bleeding, or Grade 3 or 4 gastrointestinal/variceal bleeding requiring blood transfusion, endoscopy, or surgery, within 3 months prior to the first administration of investigational product.
13. History of other acquired/congenital immunodeficiency diseases.
14. History of organ transplantation allogeneic bone marrow transplantation, or autologous hematopoietic stem cell transplantation.
15. A condition requiring systemic treatment with either corticosteroids (> 10 mg daily prednisone equivalent) within 7 days or other immunosuppressive medication(s) within 14 days of the first dose of investigational product. Subjects using physiologic replacement doses of prednisone at = 10 mg/day, or its equivalent, are eligible.
16. Active autoimmune diseases or history of autoimmune diseases that may relapse.

Note: Subjects with the following diseases are not excluded:
1. Controlled Type I diabetes.
2. Hypothyroidism (provided it is managed with hormone replacement therapy only).
3. Controlled celiac disease.
4. Skin diseases not requiring systemic treatment (eg, vitiligo, psoriasis, alopecia).
5. Any other disease that is not expected to recur in the absence of external triggering factors.
17. History or presence of metastatic brain tumors. Subjects with confirmed brain metastases are eligible for the study provided that they are asymptomatic and radiologically stable without the need for corticosteroid treatment >10 mg or seizure prophylaxis for = 4 weeks prior to first dose of investigational product.
18. Have undergone major surgeries within 4 weeks prior to first dose of investigational product.
19. Uncontrollable pleural effusion, pericardial effusion, or ascites requiring frequent drainage within 7 days prior to first dose of investigational product.
20. Under the treatment of heparin (eg, low molecular weight heparin [LMWH]) or other anticoagulants such as warfarin when administered at a therapeutic dose. Participants using prophylactic doses of heparin (LMWH) are eligible.
21. Diagnosis of any other malignancy within 2 years prior to enrollment, except for the following if adequately treated:

* Local basal cell or squamous cell carcinoma of the skin or related localized.
* Non-melanoma skin cancer.
* Carcinoma in situ of the breast or of the cervix.
* Non-muscle invasive bladder cancer.
* Low grade (Gleason 6 or below) prostate cancer undergoing surveillance with no plans for treatment intervention or previously fully resected.
22. History or presence of uncontrolled mental illness or drug abuse disorder in opinion of the Investigator.
23. The subject is expected to be non-compliant with critical study procedures and is not willing or able to adhere to the study requirements.
24. Subject is deemed inappropriate for this clinical study, or participation in this clinical study is deemed not in the best interest of the subject, at the discretion of the Investigator.
25. Other acute or chronic diseases or abnormal laboratory test that may: increase risk of study participation or investigational product administration, interfere with the interpretation of study results, and disqualify the subject for study participation in the Investigator's judgment.

Study design
Purpose of the study
Treatment
Allocation to intervention
NA
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Phase 1
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Active, not recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
5/06/2023
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
31/12/2024
Actual
Sample size
Target
48
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
QLD,SA,VIC
Recruitment hospital [1] 0 0
ICON Cancer Centre Wesley - Auchenflower
Recruitment hospital [2] 0 0
Southern Oncology Clinical Research Unit - Bedford Park
Recruitment hospital [3] 0 0
Cabrini Hospital Malvern - Malvern
Recruitment postcode(s) [1] 0 0
4066 - Auchenflower
Recruitment postcode(s) [2] 0 0
5042 - Bedford Park
Recruitment postcode(s) [3] 0 0
3144 - Malvern
Recruitment outside Australia
Country [1] 0 0
China
State/province [1] 0 0
Guangdong
Country [2] 0 0
China
State/province [2] 0 0
Hubei

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
RemeGen Co., Ltd.
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
RemeGen
Address 0 0
Country 0 0
Phone 0 0
301-284-1015
Fax 0 0
Email 0 0
[email protected]
Contact person for scientific queries

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.

Results not provided in https://clinicaltrials.gov/study/NCT05867303