Phase I Study of Oral DFP-11207 in Solid Tumors

Completed · Phase 1

Conditions studied: Solid Tumors, Cancer

In brief

This is a first-in-human, open label, single arm, sequential dose escalation and expansion study of oral DFP-11207 in patients with advanced solid tumors.

Key facts

Study ID

NCT02171221

Run by

Delta-Fly Pharma, Inc.

People needed

23

Starts

2014-06-01

Expected to finish

2018-09-13

Last updated by the study team

2019-01-29

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients must have pathologically-confirmed solid tumors, refractory after standard therapy for the disease or for which conventional systemic chemotherapy is not reliably effective or no effective therapy is available.
• Aged ≥ 18 years.
• ECOG Performance Status of 0 or 1.
• Adequate clinical laboratory values defined as:
• absolute neutrophil count ≥ 1.5 x 10\^9/L
• platelets ≥ 100 x 10\^9/L
• plasma creatinine ≤ 1.5 x upper limit of normal (ULN) for the institution
• bilirubin ≤ 1.5 x ULN
• alanine transaminase (ALT) and aspartate transaminase (AST) < 2.5 x ULN (< 5 x ULN if documented hepatic metastases)
• Absence of uncontrolled intercurrent illnesses, including uncontrolled infections, cardiac conditions, or other organ dysfunctions.
• Patients may have measurable or non-measurable disease as defined by RECIST 1.1.
• Signed informed consent prior to the start of any study specific procedures.
• Women of child-bearing potential must have a negative serum or urine pregnancy test. Male and female patients must agree to use acceptable contraceptive methods for the duration of the study and for at least one month after the last drug administration.

You may not qualify if…

• Known allergy to fluoropyrimidines or known dihydropyrimidine dehydrogenase (DPD) deficiency.
• Patients will be excluded if they have received previous chemotherapy, immunotherapy, radiotherapy or any other investigational therapy within 4 weeks (6 weeks for nitrosoureas or mitomycin C) or 5 half-lives for non-cytotoxic agents prior to this study entry.
• Extensive prior radiotherapy, more than 30% of bone marrow reserves, or prior bone marrow/stem cell transplantation.
• Any concomitant condition that in the opinion of the Investigator could compromise the objectives of this study and the patient's compliance.
• Pregnant or lactating individuals.
• Current malignancies of another type, with the exception of adequately treated in situ cervical cancer, squamous cell and basal cell skin cancer or other malignancies with no evidence of disease for 2 years or more.
• Known history of HIV, HBV or HCV infection.
• Documented or known bleeding disorder.
• Requirement for anticoagulation treatment that increases international normalized ratio (INR) or activated partial thromboplastin time (aPTT) above the normal range (low dose deep vein thrombosis (DVT) or line prophylaxis is allowed).
• Clinically evident central nervous system metastases or leptomeningeal disease not controlled by prior surgery or radiotherapy; history of seizure disorder not controlled by anti-seizure medication at the time of enrollment.
• Cardiac dysfunction defined as myocardial infarction within 6 months of study entry, New York Heart Association Class III or IV heart failure, uncontrolled dysrhythmias or poorly controlled angina.
• History of serious ventricular arrhythmia (VT or VF, ≥ 3 beats in a row), QTc ≥ 450 msec for men and 470 msec for women, or LVEF ≤ 40% by MUGA or ECHO.

Where it is running

• MD Anderson Cancer Center — Houston, Texas, United States

Full record on ClinicalTrials.gov

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