Clinical Study of Utidelone Injection in Patients With Advanced or Metastatic Solid Tumors

NCT ID: NCT04911907

Last Updated: 2023-11-08

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 120 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-01-22
• Study Completion Date: 2024-12-30

Brief Summary

This trial is an open, two-stage, multi-center, phase II clinical trial to evaluate the efficacy and safety of Utidelone in advanced solid tumors (excluding breast cancer, lung cancer, and colorectal cancer) that have failed standard of treatment or were unable to perform standard treatment.

This trial is divided into 2 stages, screening stage and expansion stage. In the screening stage, 10 patients were enrolled for each tumor type(including Squamous cell carcinoma of head and neck, Esophageal cancer, Stomach cancer, Pancreatic cancer, Cholangiocarcinoma, Ovarian cancer and Other solid tumors). Based on the results of the tumor type screening stage, the sponsor and the main investigator will have a discussion and have the alignment of tumor types to enter the expansion stage. The expansion stage will refine the inclusion / exclusion criteria and may adjust the treatment plan based on the tumor type and the combination drug selection. A total of 30-50 patients (including patients enrolled in the screening stage) were enrolled in each specified tumor type during the expansion stage.

Conditions

Solid Tumor

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Squamous cell carcinoma of head and neck: Utidelone Injection

Cohort 1 Squamous cell carcinoma of head and neck. Participants will be treated with utidelone monotherapy

Group Type: EXPERIMENTAL

utidelone injection

Intervention Type: DRUG

Utidelone monotherapy 35 mg/m2/day IV transfusing over 90 min. on day 1-day 5 of each 21 day cycle

Esophageal cancer: Utidelone injection

Cohort 2 Esophageal cancer. Participants will be treated with utidelone monotherapy.

Group Type: EXPERIMENTAL

utidelone injection

Intervention Type: DRUG

Utidelone monotherapy 35 mg/m2/day IV transfusing over 90 min. on day 1-day 5 of each 21 day cycle

Stomach cancer: Utidelone injection

Cohort 3 Stomach cancer. Participants will be treated with utidelone monotherapy.

Group Type: EXPERIMENTAL

utidelone injection

Intervention Type: DRUG

Utidelone monotherapy 35 mg/m2/day IV transfusing over 90 min. on day 1-day 5 of each 21 day cycle

Pancreatic cancer: Utidelone Injection

Cohort4 Pancreatic cancer. Participants will be treated with Utidelone monotherapy.

Group Type: EXPERIMENTAL

utidelone injection

Intervention Type: DRUG

Utidelone monotherapy 35 mg/m2/day IV transfusing over 90 min. on day 1-day 5 of each 21 day cycle

Ovarian cancer: Utidelone Injection

Cohort5 Ovarian cancer. Participants will be treated with Utidelone monotherapy.

Group Type: EXPERIMENTAL

utidelone injection

Intervention Type: DRUG

Utidelone monotherapy 35 mg/m2/day IV transfusing over 90 min. on day 1-day 5 of each 21 day cycle

Cholangiocarcinoma: Utidelone

Cohort 6 Cholangiocarcinoma. Participants will be treated with Utidelone monotherapy

Group Type: EXPERIMENTAL

utidelone injection

Intervention Type: DRUG

Utidelone monotherapy 35 mg/m2/day IV transfusing over 90 min. on day 1-day 5 of each 21 day cycle

Other solid tumors: Utidelone Injection

Cohort 7 Other solid tumors. Participants will be treated with Utidelone monotherapy

Group Type: EXPERIMENTAL

utidelone injection

Intervention Type: DRUG

Utidelone monotherapy 35 mg/m2/day IV transfusing over 90 min. on day 1-day 5 of each 21 day cycle

Interventions

utidelone injection

Utidelone monotherapy 35 mg/m2/day IV transfusing over 90 min. on day 1-day 5 of each 21 day cycle

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Histologically or cytologically documented locally-advanced and/or metastatic solid malignancy (including Squamous cell carcinoma of head and neck, Esophageal cancer, Stomach cancer, Pancreatic cancer, Cholangiocarcinoma, Ovarian cancer and Other solid tumors) that is incurable, and has failed prior standard therapy or for which standard therapy is not appropriate.

2. Have measurable disease based on Response Criteria in Solid Tumors Version 1.1 (RECIST 1.1)

3. Age 18 -70 years old

4. ECOG performance status of 0-1

5. Life expectancy≥ 3 months

6. Basically normal results from routine blood test within 1 week prior to enrollment

1. Absolute neutrophil count (ANC) >= 1.5 x 10^9/L

2. Hemoglobin >= 9 g/dL

3. Platelets >= 80 x 10^9/L

7. Basically normal liver and renal functions within 1 week prior to enrollment

1. total bilirubin =< 1.5 x ULN with direct bilirubin within normal range

2. Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) =< 3 x ULN (ALT and AST =< 5 x ULN is acceptable if liver metastases are present)

3. Creatinine clearance>=50 ml/min

8. Women and men of childbearing potential must agree to take effective contraceptive measures during the study and within six months after the last treatment. Female patients must have negative urinary pregnancy test within 7 days before the first treatment (postmenopausal women must have no menstruation for at least 12 months before they are considered unable to conceive)

9. Patients who give written informed consent with good compliance.

Exclusion Criteria

1. Received chemotherapy, radiotherapy, biological therapy, endocrine therapy, immunotherapy and other anti-tumor treatments within 4 weeks prior to enrollment while participating in this trial, except for the following items:

1. Nitrosourea or mitomycin C is within 6 weeks before the first dosage of the study drug;

2. Oral fluorouracil and small molecule targeted drugs are 2 weeks before the first use of the study drug or 5 half-life periods of the drug (whichever is longer);

3. The traditional Chinese medicine with anti-tumor indication is within 2 weeks before the first use of the research medicine.

2. Received other unlaunched clinical research drugs or treatment within 4 weeks before the first dosage of the research drug.

3. Have undergone major organ surgery (excluding needle biopsy) or experienced significant trauma within 4 weeks prior to the first dosage of study drug, or require elective surgery during the trial period.

4. Symptomatic peripheral neuropathy CTCAE 5.0 grade evaluation ≥ grade 2

5. With severe allergies to castor oil, or have had serious adverse reactions with anti-microtubule drugs in the past

6. Patients of pregnancy or breast feeding

7. Patients with AEs caused by any previous treatment (including systemic and local treatment) that have not yet restored to GRADE 1 (excluding hair loss)

8. Patient with known active central nervous system (CNS) metastases and/or carcinomatous meningitis.

9. Patients with active infections and currently need systemic anti-infective treatment

10. Patient with immunodeficiency, including a positive HIV antibody test.

11. Patients with history of active hepatitis B (hepatitis B virus titer> ULN), allow prophylactic antiviral treatment other than interferon; have a history of hepatitis C virus infection (hepatitis C antibody positive).

12. Patients with history of serious cardiovascular and cerebrovascular diseases.

13. Patients with mental disorders or patients with poor compliance.

14. Patients not fitted for this study determined by the investigators.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Chengdu Biostar Pharmaceuticals

INDUSTRY

Sponsor Role: collaborator

Beijing Biostar Pharmaceuticals Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

JIN LI, MD

Role: PRINCIPAL_INVESTIGATOR

Shanghai Tongji University Affiliated Oriental Hospital

Locations

Luhe Hospital, Capital Medical University

Beijing, , China

Site Status: RECRUITING

Obstetrics and Gynecology Hospital, Capital Medical University

Beijing, , China

Site Status: RECRUITING

Shanghai East Hospital of Tongji University

Shanghai, , China

Site Status: RECRUITING

Countries

China

Central Contacts

RONGGUO QIU, PhD

Role: CONTACT

rqiu2001@yahoo.com

01186-5631-5388

Facility Contacts

Dong Yan, MD

Role: primary

Yumei Wu, MD

Role: primary

Jin Li, MD

Role: primary

Other Identifiers

BG01-2002

Identifier Type: -

Identifier Source: org_study_id