A Phase II Study to Evaluate the Efficacy and Safety of TLC388 in Advanced/Metastatic RCC Patients

NCT ID: NCT01831973

Last Updated: 2018-06-26

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 18 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-11-30
• Study Completion Date: 2017-02-21

Brief Summary

INVESTIGATIONAL PRODUCT:

TLC388 (Lipotecan*) *Lipotecan is a drug product of TLC388 HCl.

PHASE OF DEVELOPMENT:

Phase II

No. OF PATIENTS:

Approximately 40 (Stage I: 15 evaluable patients, Stage II: 25 evaluable patients)

STUDY OBJECTIVES:

Primary

• To evaluate non-progression disease (non-PD) rate at the end of cycle 6

Secondary

• To evaluate progression free survival (PFS)
• To evaluate overall survival (OS)
• To evaluate the duration of non-PD
• To evaluate objective response rate (ORR; where ORR= CR+PR) and duration
• To evaluate the safety profile of TLC388
• To evaluate change in health-related quality of life (HRQOL) at the end of cycle 6

STUDY DESIGN:

This is a Phase II, open-label, single-arm, multi-centre study to evaluate TLC388 monotherapy in patients with locally advanced and/or metastatic renal cell carcinoma (RCC).

Detailed Description

A Phase II, open-label, single-arm, multi-center study to evaluate TLC388 monotherapy in patients with locally advanced and/or metastatic RCC. The study consisted of a Screening/Baseline Period, a Treatment Period and a post-treatment Follow-Up Period for PFS and OS.

Patients were to be recruited at two stages. Stage I recruited 15 evaluable patients, who had completed at least 2 cycles of treatment with one tumor assessment. If ≤ 5 patients did not develop PD at the end of cycle 6 per RECIST, no patients were to be recruited for Stage II and the study was to be closed. If > 5 patients did not develop PD at the end of cycle 6, a total of 40 evaluable patients (additional 25 evaluable patients for Stage II) were to be recruited thereafter.

Conditions

Advanced/Metastasis Renal Cell Carcinoma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Lipotecan, injection for chemotherapy

Patients receive TLC388 (50 mg/m2) given as a 30-minute IV infusion, on Days 1, 8, and 15 of a 28-day cycle.

Group Type: EXPERIMENTAL

Lipotecan

Intervention Type: DRUG

Interventions

Lipotecan

Intervention Type: DRUG

Other Intervention Names

TLC388

Eligibility Criteria

Inclusion Criteria

1. Adult patients defined by age ≥ 18 years

2. Histologically confirmed Renal cell carcinoma (RCC)

3. Locally advanced or metastatic RCC. Locally advanced RCC: defined as a stage T3/T4 disease, not amenable to curative surgery or radiation therapy, with involvement of renal vein/vena cava/peripelvic and perirenal fat/adrenal gland, or invasion beyond Gerota's fascia. Metastatic RCC: equivalent to Stage IV RCC, according to American Joint Committee on Cancer (AJCC) staging

4. Eastern Collaborative Oncology Group (ECOG) Performance Status of ≤ 2. But for the patient with failure of ≥ 2 prior target therapies, ECOG should be ≤ 1.

5. Documented RCC disease with measurable or non-measurable lesion on imaging by RECIST v1.1 (Response Evaluation Criteria in Solid Tumors) criteria

6. Documented treatment failure of at least 1 prior target therapy (sorafenib, sunitinib pazopanib or other VEGF TKI, bevacizumab, temsirolimus, everolimus or other mTOR inhibitor) for advanced or metastatic RCC. If treatment-naïve, patients with poor prognosis features according to Memorial Sloan-Kettering Cancer Centre (MSKCC) risk criteria are acceptable

7. Any acute or chronic adverse effects of prior therapy have resolved to <Grade 2 as determined by CTCAE v4.0 criteria

8. Laboratory values at screening:

• Absolute neutrophil count ≥ 1,500 /mm3;
• Platelets ≥ 100,000 /mm3;
• Hemoglobin ≥ 9.0 g/dL;
• Total bilirubin ≤ 1.5 times the upper limit of normal;
• AST (SGOT) ≤ 2.5 times the upper limit of normal;
• ALT (SGPT) ≤ 2.5 times the upper limit of normal;
• Serum creatinine ≤ 2 times the upper limit of normal;

Exclusion Criteria

1. Pregnancy or lactation. Women of childbearing potential must have a negative serum pregnancy test within 7 days prior to enrolment. Male and female patients of childbearing potential must agree to use appropriate birth control (barrier methods with spermicides, oral or parenteral contraceptives and/or intrauterine devices) during the entire duration of the study, or the patient must be surgically sterile (with documentation in the patient's medical records)

2. Receipt of any chemotherapy for RCC

3. Had cardiac angioplasty or stenting event, myocardial infarction or unstable angina within 3 months of study entry

4. Persistent QTc >450 ms for males, or >470 ms for females, according to Fridericia's correction

5. Patients with Grade 3 or greater hyponatremia at screening

6. History of Class III or IV congestive heart failure according to New York Heart Association (NYHA) classification

7. History of another malignancy, except for non-basal-cell carcinoma of skin or carcinoma-in-situ of the uterine cervix, and not disease free ≥5 years

8. History or presence of central nervous system (CNS) metastasis or leptomeningeal tumors as documented by CT or MRI scan, analysis of cerebrospinal fluid or neurological exam

9. History of human immunodeficiency virus infection

10. Presence of active, uncontrolled infection

11. Radiotherapy received within 4 weeks prior to baseline

12. Use of any investigational agents within 4 weeks of baseline

13. Major surgery within 4 weeks prior to baseline

14. Receipt of radiotherapy to >25 % of bone marrow

15. Concomitant treatment with, or anticipated use of, pharmaceutical or herbal agents which are potent inhibitors or inducers of cytochrome P450 enzymes (Appendix D1), unless approved by the Sponsor

16. Uncontrolled intercurrent illness that would jeopardize patient safety, or interfere with the objectives of the protocol, or limit patient compliance with study requirements, as determined by the Investigator

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Taiwan Liposome Company

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Dr. Yvonne Shi

Role: STUDY_DIRECTOR

Taiwan Liposome Company

Locations

Chang Gung Memorial Hospital. Kaohsiung Branch

Kaohsiung City, , Taiwan

China Medical University Hospital

Taichung, , Taiwan

Taichung Veterans General Hospital

Taichung, , Taiwan

National Taiwan University Hospital

Taipei, , Taiwan

Chang Gung Memorial Hospital: LinKou Branch

Taoyuan District, , Taiwan

Countries

Taiwan

Other Identifiers

TLC388.3

Identifier Type: -

Identifier Source: org_study_id