Oral Paclitaxel Trial In Recurrent and Metastatic Breast Cancer As 1st Line Therapy

NCT ID: NCT03315364

Last Updated: 2024-07-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

PHASE2/PHASE3

Total Enrollment

549 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-12-18

Study Completion Date

2025-12-31

Brief Summary

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To compare and evaluate the efficacy and safety of Liporaxel® solution (oral paclitaxel) and Taxol® (IV paclitaxel) on recurrent or metastatic breast cancer.

Detailed Description

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Conditions

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Recurrent or Metastatic Breast Cancer

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

1. Phase II clinical trial

* Multicenter, Open-label, Single arm, Simon's optimal two-stage design
2. Phase III clinical trial

* Multicenter, Prospective Randomized Open-label Blinded Endpoint (PROBE) design
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Liporaxel® (oral paclitaxel)

* 28 days (4 weeks) will be set as one cycle of administration and Liporaxel® will be administered for 3 weeks, twice a day, every morning and evening (D1, D8, D15) and will take a week off on 4th week.
* Liproaxel® 200mg/m2 will be orally administered twice a day (morning, evening) 1 hour after meal for D1, D8, D15 of every cycle. 10 hour-interval is recommended for between each administration.

Group Type EXPERIMENTAL

Oral paclitaxel

Intervention Type DRUG

Oral administration on D1, D8 and D15 of 4-week cycle until progression, unacceptable toxicity or withdrawal of informed concent

Taxol® (IV paclitaxel)

* 28 days (4 weeks) will be set as one cycle and for every 3 week administration, 1 week off dose period will be given.
* Taxol® 80mg/m2 will be administered via IV and it must be diluted before drip administration. Dilute with 0.9% sodium chloride injection solution to make final concentration of 0.3-1.2 mg/mL.

Group Type ACTIVE_COMPARATOR

Paclitaxel injection

Intervention Type DRUG

Premedication, intravenous infusion on D1, D8 and D15 of 4-week cycle until progression, unacceptable toxicity or withdrawal of informed concent

Interventions

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Oral paclitaxel

Oral administration on D1, D8 and D15 of 4-week cycle until progression, unacceptable toxicity or withdrawal of informed concent

Intervention Type DRUG

Paclitaxel injection

Premedication, intravenous infusion on D1, D8 and D15 of 4-week cycle until progression, unacceptable toxicity or withdrawal of informed concent

Intervention Type DRUG

Other Intervention Names

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Liporaxel® Taxol®

Eligibility Criteria

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Exclusion Criteria

* Histologically or cytologically confirmed to have recurrent, or metastatic breast cancer.
* Measurable disease (revised RECIST, version 1.1).
* Hormone receptor (ER/PR) positive or negative, HER2 negative.
* Subjects were eligible for the study regardless of their previous lines of endocrine therapy.
* No prior chemotherapy is allowed in metastatic disease.
* Subjects who administrated the last dose of taxane class drug ≥12months ago as from the first administration day.
* ECOG performance status ≤1.
* Neuropathy grade \<2.
* Subjects with central nervous system metastasis should be excluded.
Minimum Eligible Age

19 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Daehwa Pharmaceutical Co., Ltd.

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Sung-bae Kim, M.D., Ph.D

Role: PRINCIPAL_INVESTIGATOR

Asan Medical Center

Locations

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Oncology Complex Center - Burgas'' Ltd., Medical Oncology Department

Burgas, , Bulgaria

Site Status

Multi-profile Hospital for Active Treatment Uni Hospital Ltd. Medical Oncology Department

Panagyurishte, , Bulgaria

Site Status

Medical Center Nadezhda Clinical" Ltd.,

Sofia, , Bulgaria

Site Status

Anhui Cancer Hospital

Hefei, Anhui, China

Site Status

Cancer Hospital Chinese Academy Of Medical Sciences

Beijing, Beijing Municipality, China

Site Status

Sun Yat-sen University Cancer Center

Guangzhou, Guangdong, China

Site Status

The First Affiliated Hospital Of Hainan Medical College

Haikou, Hainan, China

Site Status

Harbin Medical University Cancer Hospital

Harbin, Heilongjiang, China

Site Status

Tianjin Cancer Hospital

Zhengzhou, Henan, China

Site Status

Jiangsu Cancer Hospital

Nanjing, Jiangsu, China

Site Status

Jiangsu Province Hospital

Nanjing, Jiangsu, China

Site Status

First Affiliated Hospital of Jilin University

Changchun, Jilin, China

Site Status

Liaoning Cancer Hospital

Shenyang, Liaoning, China

Site Status

Shangdong Cancer Hospital

Jinan, Shandong, China

Site Status

Linyi Cancer Hospital

Linyi, Shandong, China

Site Status

Fudan University Shanghai Cancer Center

Shanghai, Shanghai Municipality, China

Site Status

The First Affiliated Hospital of Xi'an Jiaotong university

Xi’an, Shanxi, China

Site Status

West China School Of Medicine Sichuan University

Chengdu, Sichuan, China

Site Status

Zhejiang Cancer Hospital

Hangzhou, Zhejiang, China

Site Status

Zhejiang University School Of Medicine Sir Run Run Shaw Hospital

Hangzhou, Zhejiang, China

Site Status

Henan Cancer Hospital

Zhengzhou, , China

Site Status

Tolna County Balassa János Hospital

Szekszárd, , Hungary

Site Status

Szent Borbála Hospital

Tatabánya, , Hungary

Site Status

Institute for Oncology and Radiology of Serbia

Belgrade, , Serbia

Site Status

Clinical Hospital Center Bežanijska Kosa, Department of Oncology

Belgrade, , Serbia

Site Status

Oncology Institute of Vojvodina

Kamenitz, , Serbia

Site Status

Health Center Kladovo, Oncology Department

Kladovo, , Serbia

Site Status

Clinical Center Kragujevac Center of Oncology and Radiotherapy

Kragujevac, , Serbia

Site Status

General Hospital Krusevac, Outpatient Clinic for chemotherapy

Kruševac, , Serbia

Site Status

Clinical Center Niš, Clinic for Oncology

Niš, , Serbia

Site Status

Wonju Severance Christian Hospital

Wŏnju, Gangwon-do, South Korea

Site Status

National Cancer Center

Goyang-si, Gyeonggi-do, South Korea

Site Status

Cha University Cha Bundang Medical Center

Seongnam-si, Gyeonggi-do, South Korea

Site Status

Ajou University Hospital

Suwon, Gyeonggi-do, South Korea

Site Status

Chungbuk National University Hospital

Cheongju-si, North Chungcheong, South Korea

Site Status

Inje University Haeundae Paik Hospital

Busan, , South Korea

Site Status

Kosin University Gospel Hospital

Busan, , South Korea

Site Status

Pusan National University Yangsan Hospital

Busan, , South Korea

Site Status

Keimyung University Dongsan Medical Center

Daegu, , South Korea

Site Status

Konyang University Hospital

Daejeon, , South Korea

Site Status

Gang Neung Asan Hospital

Gangneung, , South Korea

Site Status

Gachon University Gil Medical Center

Incheon, , South Korea

Site Status

Korea University Anam Hospital

Seoul, , South Korea

Site Status

Seoul National University Hospital

Seoul, , South Korea

Site Status

Yonsei University Severance Hospital

Seoul, , South Korea

Site Status

Asan Medical Center

Seoul, , South Korea

Site Status

Samsung Medical Center

Seoul, , South Korea

Site Status

Korea University Guro Hospital

Seoul, , South Korea

Site Status

Catholic University of Korea Seoul ST. Mary's Hospital

Seoul, , South Korea

Site Status

Gangnam Severance Hospital

Seoul, , South Korea

Site Status

Uijeongbu ST. Mary's Hospital

Uijeongbu-si, , South Korea

Site Status

Countries

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Bulgaria China Hungary Serbia South Korea

References

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Kim SB, Seo JH, Ahn JH, Kim TY, Kang SY, Sohn J, Yang Y, Park KH, Moon YW, Lim S, Kang MJ, Yoon KE, Cho HJ, Lee KS. Phase II study of DHP107 (oral paclitaxel) in the first-line treatment of HER2-negative recurrent or metastatic breast cancer (OPTIMAL study). Ther Adv Med Oncol. 2021 Dec 15;13:17588359211061989. doi: 10.1177/17588359211061989. eCollection 2021.

Reference Type DERIVED
PMID: 34925553 (View on PubMed)

Other Identifiers

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107CS-5

Identifier Type: -

Identifier Source: org_study_id

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