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Completed Phase 2 Interventional

Oral Paclitaxel Efficacy Safety and PK in Recurrent and Metastatic Breast Cancer

ClinicalTrials.gov ID: NCT03326102

Public ClinicalTrials.gov record NCT03326102. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 8:05 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multi-national,Multi-center, Open-label, Phase 2 Clinical Trial to Evaluate the Efficacy, Safety and Pharmacokinetics of DHP107 (Liporaxel®,Oral Paclitaxel) Compared to IV Paclitaxel in Patients With Recurrent or Metastatic Breast Cancer(OPERA)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The objective of this study is to evaluate the efficacy, safety and pharmacokinetics of DHP107 (Oral Paclitaxel, Korea brand name: Liporaxel®) compared to IV Paclitaxel in patients with Recurrent or Metastatic Breast Cancer.

Study identification

NCT ID
NCT03326102
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Daehwa Pharmaceutical Co., Ltd.
Industry
Enrollment
72 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 6, 2018 (Actual)
Primary completion
Dec 13, 2022 (Actual)
Completion
Dec 13, 2022 (Actual)
Last update posted
Feb 16, 2024

2018 – 2022

United States locations

U.S. sites
12
U.S. states
9
U.S. cities
11
Facility City State ZIP Site status
California Research Institute (CRI) Los Angeles California 90027 —
University of California San Francisco (UCSF) San Francisco California 94115 —
Boca Raton Regional Hospital (BRRH) Boca Raton Florida 33486 —
ASCLEPES Research Center(ARC) Weeki Wachee Florida 34607 —
Saint Luke's Cancer Institute(SLCI) Kansas City Kansas 64111 —
University of Kansas Medical Center(KUMC) Kansas City Kansas 66160 —
Anne Arundel Health System Research Institute (AAHS) Annapolis Maryland 21401 —
Massachusetts General Hospital(MGH) Boston Massachusetts 02114 —
Michigan Center of Medical Research(MCMR) Farmington Hills Michigan 48334 —
Metro-Minnesota Community Oncology Research Consortium (MMCORC) Minneapolis Minnesota 55426 —
Nevada Cancer Research Foundation (NCRF) Las Vegas Nevada 89106 —
University of Pittsburgh Medical Center (UPMC) Pittsburgh Pennsylvania 15232 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03326102, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 16, 2024 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03326102 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →