Food Effect on Pharmacokinetics and SafEty of DHP107 (Liporaxel®) FEEL Study

Advanced Solid Tumor Clinical Trial

— FEEL  

Official title:

A Randomized, Open-label, Two-way Crossover Clinical Trial to Evaluate the Food Effect on Pharmacokinetics and Safety of DHP107 (Oral Paclitaxel, Liporaxel®) in Patients With Advanced Solid Tumors (FEEL) / EudraCT no : 2020-004976-16

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT04675528
• Other study ID #: 107CS-7
• Status: Not yet recruiting
• Phase: Phase 1
• Start date: January 2021
• Est. completion date: March 2022

Study information

• Verified date: December 2020
• Source: Daehwa Pharmaceutical Co., Ltd.
• Contact: Erika Hitre, M.D., Ph.D
• Phone: +36-1-22-48-763
• Email: hitre[@]oncol.hu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To evaluate the food effect on pharmacokinetics of DHP107 in patients with advanced solid tumors.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 24
• Est. completion date: March 2022
• Est. primary completion date: September 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Subjects who are =18 years of age on the date of written informed consent.

2. Subjects with histologically or cytologically confirmed advanced solid tumors including but not limited to the listed below for which paclitaxel monotherapy has been determined an appropriate therapy at the investigator's discretion.

• Angiosarcoma

• Bladder cancer

• Breast cancer

• Cervical cancer

• Head and neck cancer (if no difficulty with swallowing)

• Kaposi's sarcoma

• Lung cancer

• Ovarian cancer

3. Subjects who have a life expectancy of =12 weeks.

4. Subjects who are able to take oral medication.

5. Subjects who have a performance status of = 2 on the Eastern Cooperative Oncology Group (ECOG) scale.

6. Subjects who have evaluable disease according to the Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST version 1.1).

7. Subjects who have adequate organ functions as indicated by the following laboratory values:

8. Subjects who are willing and able to comply with scheduled visits, treatment plans, laboratory tests, and procedures.

9. Subjects who have voluntarily agreed to participate by giving written informed consent.

10. Women of childbearing potential who have negative pregnancy test results at the screening visit and men with female partners of childbearing potential must agree to use adequate contraception for the duration of the trial and up to 90 days after last dose of study drug

Exclusion Criteria:

1. Subjects who have history of severe hypersensitive reaction to the active ingredient or any excipients of DHP107.

2. Subjects with following surgical history/medical conditions that may affect drug absorption:

3. Subjects who developed cardiovascular disease (unstable angina, myocardial infarction, stroke, and transient ischemic attack) within 24 weeks prior to study entry, which is deemed to be clinically significant by the investigator.

4. Subjects with known active hepatitis B or C infection, or hepatobiliary disease, or known history of immunodeficiency virus infection (However, subjects with Gilbert's Syndrome, asymptomatic gallstones, or stable chronic liver disease are, at the discretion of the investigator, eligible for the study. Subjects who are hepatitis B carriers may be eligible if they are on antiviral therapy 2 weeks prior to study entry).

5. Subjects with neuropathy grade > 2 based on CTCAE v5.0 at the time of study entry.

6. Subjects with uncontrolled medical or mental illness that, in the investigator's judgement, could affect treatment tolerability or compliance.

7. Subjects diagnosed with other malignant primary tumor with an exception of the following:

• Malignancy diagnosed at least 5 years previously without evidence of recurrence or persistent disease

• The complete excision of basal/squamous cell carcinoma or papillary thyroid carcinoma or the complete treatment of cervical intraepithelial neoplasia or other in situ carcinoma

8. Subjects with symptomatic or unstable, untreated metastases to the central nervous system (CNS) at the time of screening ('Unstable' means worsening of symptoms within 4 weeks prior to screening).

9. Subjects who are currently receiving alternative cytotoxic agents, regular systemic corticosteroids and medications that could influence drug absorption (e.g. H2-antihistamines, antacids, metoclopramide and charcoal) within 4 weeks prior to entry into the study (C1D1).

10. Subjects who are currently receiving (or unable to stop use the 3 days before the first dose of DHP107 and throughout the study) prescription or non-prescription medications or other products known to be moderate or potent inhibitors/inducers of CYP3A4, P-gp, or CYP2C8.

11. Subjects who cannot intake whole high fat meal offered.

12. Pregnant or breastfeeding women.

13. Subjects who have received any investigational drugs or devices within 4 weeks before the first day of study treatment (C1D1)

Related Conditions & MeSH terms

• Advanced Solid Tumor

Intervention

Drug:
• DHP107(Oral paclitaxel)
DHP107 200 mg/m2 orally twice daily on Days 1, 8, and 15 in every 28 days (On food effect study day, DHP107 200 mg/m2 orally once daily on Days 1, 8 of Cycle 1 with fasted or fed condition according to the assigned sequence)

Locations

Country	Name	City	State
Hungary	National Institute of Oncology	Budapest
Hungary	University of Semmelweis, 1st Internal Medicine Clinic, Department of Clinical Pharmacology	Budapest
Hungary	University of Debrecen-Clinical Center, Internal Medicine Clinic, Department of Clinical Pharmacology	Debrecen

Sponsors (1)

Lead Sponsor	Collaborator
Daehwa Pharmaceutical Co., Ltd.

Country where clinical trial is conducted

Hungary, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	• Cmax	The primary endpoints of this trial are the ratio of geometric means of the following pharmacokinetic parameters following DHP107 administration fed with fasting condition	Day 1 and Day 8 of Cycle 1(each cycle is 28 days)
Primary	• Tmax	and the median difference of the following pharmacokinetic parameters following DHP107 administration fed with fasting condition:	Day 1 and Day 8 of Cycle 1(each cycle is 28 days)