A Study DHP107, a Novel Oral Paclitaxel Formulation, in Patients With Advanced Solid Tumours or Gastric Cancer

NCT ID: NCT02890511

Last Updated: 2017-02-13

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 28 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-08-31
• Study Completion Date: 2012-10-31

Brief Summary

A study of DHP107, a novel oral paclitaxel formulation, to determine maximum tolerated dose and recommended dose for phase II trial in patients with advanced solid cancer and explore efficacy of DHP107 in patients with gastric cancer

Detailed Description

1. Primary objective To determine the maximum tolerated dose and the recommended dose for phase 2 clinical trial for the repeated administration of DHP107 (oral paclitaxel) on advanced solid cancer patients

2. Secondary objectives

• To identify the dose limiting toxicity and the safety (toxicity) of DHP107
• To evaluate the efficacy (tumor response rate) of DHP107
• To assess pharmacokinetic (PK) characteristics of DHP107

Conditions

Solid Tumor; Stage IV Gastric Cancer

Study Design

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

Study Groups

DHP107(Oral paclitaxel)

• Phase I (determining MTD) The patients diagnosed with either advanced or metastatic solid cancers were enrolled. The administered dose was escalated in a step-wise manner by an increment of 2 x 50 mg/m2 at each dose level. Three patients were treated for toxicity evaluation for each dose level.
• Phase IIa (efficacy evaluation) The safety and efficacy of the corresponding dose was investigated more closely by increasing the patient number to 6 or more patients in the dose tentatively determined as recommended dose for phase IIa clinical trial.

Group Type: EXPERIMENTAL

Paclitaxel

Intervention Type: DRUG

Oral administration on day 1,8,15 of 4-week cycle until progression, unacceptable toxicity or withdrawal of informed consent.

Interventions

Paclitaxel

Oral administration on day 1,8,15 of 4-week cycle until progression, unacceptable toxicity or withdrawal of informed consent.

Intervention Type: DRUG

Other Intervention Names

DHP107

Eligibility Criteria

Inclusion Criteria

1. Patients between 18 and 70 years old

2. Patients prognosed with advanced or metastatic solid cancer by histopathology or cytology analysis who have no available standard therapy or who have failed at least once with the standard therapy

3. Adequate bone marrow function, liver function and adequate kidney function

4. Eastern Cooperative Oncology Group performance status ≤ 2

5. Life expectancy of 3 month or more

6. Written informed consent

Exclusion Criteria

1. Major infectious or neurological disease and bowel obstruction

2. Brain metastasis or hematologic malignancy

3. Patients who underwent surgery, radiation therapy, hormone or chemotherapy within 4 weeks prior to the beginning of investigational drug administration

4. Patients with the history of failure to the taxane line of chemotherapy (with the exception of when it was used before 6 month as adjuvant therapy or when the treatment was discontinued due to docetaxel related side effect)

5. Patients who are required to continuously take P-gp (P-glycoprotein) suppressor, immune suppressor, proton-pump inhibitor or H2-receptor antagonist during clinical trial period

6. Patients deemed by the investigator to suffer from severe heart disease (myocardial infarction, congestive heart failure, arrythmia accompanying drastic changes on ECG, severe or unstable angina pectoris, or other severe heart disease) or accompanying other severe internal diseases (such as uncontrollable diabetes, chronic obstructive pulmonary disease)

7. Patients with prior history of participating in a clinical trial within 30 days from registration for current clinical trial

8. Patient with history of alcohol or drug abuse in the recent 3 months

9. Pregnant women, nursing mothers, or patients of childbearing age who did not agree to contraception (both men and women)

10. Patients with (or suspected to have) abnormality in bile acid secretion (e.g.,. patients with resected gallbladder)

11. Patients who had a history of serious gastrointestinal bleeding, or with diseases that could affect the absorption of oral medication (malabsorption syndrome, active peptic ulcer)

12. Patients with history of severe hypersensitive reaction to active ingredient and excipient of the investigational drug

13. Patient who are in a state that is deemed inappropriate to participate in the clinical trial by the investigator

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Daehwa Pharmaceutical Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Yoon-Koo Kang, M.D., Ph.D

Role: PRINCIPAL_INVESTIGATOR

Asan Medical Center

Locations

Asan Medical Center, University of Ulsan College of Medicine

Seoul, , South Korea

Countries

South Korea

References

Ryu MH, Ryoo BY, Kim TW, Kim SB, Lim HS, Bae KS, Park SR, Jo YW, Cho HJ, Kang YK. A Phase I/IIa Study of DHP107, a Novel Oral Paclitaxel Formulation, in Patients with Advanced Solid Tumors or Gastric Cancer. Oncologist. 2017 Feb;22(2):129-e8. doi: 10.1634/theoncologist.2016-0273. Epub 2017 Feb 14.

Reference Type: DERIVED

PMID: 28196905 (View on PubMed)

Other Identifiers

107CS-2

Identifier Type: -

Identifier Source: org_study_id