Phase1 Study of Gemcitabine HCl Oral Formulation(D07001-F4) in Patients With Advanced Solid Malignancies and Malignant Lymphomas

NCT ID: NCT01800630

Last Updated: 2019-07-08

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 37 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2013-04-30
• Study Completion Date: 2016-03-31

Brief Summary

Open-label Phase 1 sequential dose-escalation study of 10 increasing doses (3 to 6 patients each)to determine and characterize the DLTs and MTD of gemcitabine HCl oral formulation (D07001-F4). Patients will be assigned to receive oral D07001-F4 on Days 1, 3, 5, 8, 10, and 12 of 4 21-day cycles each to further characterize safety and tolerability.

Conditions

Advanced Solid Malignancies; Malignant Lymphomas

Study Design

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

Study Groups

Gemcitabine HCl Oral Formulation (D07001-F4)

Subjects will receive a single 5-mg (nontherapeutic) dose of gemcitabine (Gemzar®) via an IV push and then treated with Gemcitabine HCl Oral Formulation (D07001-F4)according to assigned cohort (2 mg to 80 mg) on Day 1, 3, 5, 8, 10, and 12 of 4 21-day cycles study treatment period.

Group Type: EXPERIMENTAL

Gemcitabine HCl Oral Formulation

Intervention Type: DRUG

Interventions

Gemcitabine HCl Oral Formulation

Intervention Type: DRUG

Other Intervention Names

D07001-F4

Eligibility Criteria

Inclusion Criteria

• Male or female patients aged 20 years and older
• Signed and dated informed consent form
• Patients with advanced solid malignancies and malignant lymphomas with histological or pathologic confirmation who have failed standard therapies or for which no standard therapy exists
• Both measurable and non-measurable disease allowed (measurable disease per RECIST, version 1.1, or Revised Response Criteria for Malignant Lymphoma [Cheson criteria])
• World Health Organization (WHO) performance status 0 to 2
• At least 28 days have elapsed (before screening) since the patient's prior systemic therapy, radiotherapy, or any major surgery (excluding diagnostic biopsy or venous access device placement)
• Patient has

• Absolute neutrophil count (ANC) ≥ 1500 cells/mm³
• Platelet count ≥ 75,000 cells/mm³
• Hemoglobin ≥ 9 g/dL.
• Patient has adequate liver function, demonstrated by:

• Aspartate transaminase (AST) and alanine transaminase (ALT) ≤ 2.5*the upper limit of normal (ULN) (≤ 5.0*ULN in case of liver metastasis)
• Total bilirubin ≤ 1.5 mg/dL (unless due to Gilbert's syndrome)
• Albumin ≥ 2.5 g/dL
• International normalized ratio (INR) < 1.5
• Patient has adequate renal function:

• Serum creatinine ≤ 1.5*ULN.
• Patient has a life expectancy > 12 weeks.
• If a woman of child-bearing potential, patient has a negative pregnancy test and is not breast feeding.
• If a woman of child-bearing potential, patient is using a medically acceptable form as two barrier methods (e.g., combination of condom, diaphragm, intrauterine device), hormonal contraception (estrogen or progesterone agents) or one barrier method in combination with spermicide. Birth control is required 1 month prior to screening, for the duration of their study participation, and for 1 month after the end of the study; female partners of male patients will also adhere to similar birth control methods
• Patient is willing to comply with protocol-required visit schedule and visit requirements

• Patient has received radiotherapy of more than 10 Gy within 6 months of screening.
• Patient has a history of drug or alcohol abuse within last year.
• Patient has documented cerebrovascular disease.
• Patient has a seizure disorder not controlled on medication (based on decision of Investigator).
• Patient received an investigational agent within 28 days of screening
• Patient received systemic treatment for infection within 14 days of screening.
• Patient has known human immunodeficiency virus (HIV) infection.
• Patient has hepatitis B virus (HBV) and/or hepatitis C virus (HCV) infection in medical history.
• Patient has received yellow fever vaccine and other live attenuated vaccines within the last 4 weeks
• Patient has any other serious medical condition that, in the Investigator's medical opinion, would preclude safe participation in a clinical trial.
• Patients have gastrointestinal disease/prior surgery that may interfere with adequate oral therapy absorption
• Patients after allogeneic stem cell transplantation
• Patients with less than 12 months from autologous stem cell transplantation

Exclusion Criteria

• Patient is receiving full-dose (therapeutic) anticoagulation therapy.
• Patient is intolerant or allergic or has a known hypersensitivity to gemcitabine
• Patient has clinically significant cardiovascular disease (for example: uncontrolled hypertension, unstable angina, congestive heart failure, or New York Heart Association Grade 2 or greater).
• Patient has uncontrolled serious cardiac arrhythmia.
• Patient has known brain metastases or any leptomeningeal metastases.

• Minimum Eligible Age: 20 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

InnoPharmax Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Chia-Chi Lin, MD

Role: PRINCIPAL_INVESTIGATOR

National Taiwan University Hospital

Wu-Chou Su, MD

Role: PRINCIPAL_INVESTIGATOR

National Cheng-Kung University Hospital

Yee Chao, MD

Role: PRINCIPAL_INVESTIGATOR

Taipei Veterans General Hospital, Taiwan

Locations

National Cheng Kung University Hospital

Tainan City, , Taiwan

National Taiwan University Hospital

Taipei, , Taiwan

Taipei Veterans General Hospital

Taipei, , Taiwan

Countries

Taiwan

Other Identifiers

HR-12-001

Identifier Type: -

Identifier Source: org_study_id