Fimepinostat, Combination HDAC and Pi3-kinase Inhibitor Tumor-Directed Therapy for Cushing Disease

NCT ID: NCT05971758

Last Updated: 2025-07-04

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-01-16
• Study Completion Date: 2029-01-31

Brief Summary

Supported by the pre-clinical data (summarized in Research Strategy), the investigators propose that Fimepinostat is an ideal candidate drug in the treatment and intervention of patients with Cushing Disease. The investigators propose a pilot, short-term (4 weeks) phase II single-center study to demonstrate the safety and efficacy of Fimepinostat in the treatment of patients with de novo, persistent, and/or recurrent CD recruited at the University of California, Los Angeles. The trial will have a 2-arm design and will simultaneously examine two different doses of Fimepinostat. The study will allow the investigators to determine the efficacy and safety of these doses in the treatment of CD and guide dose selection for subsequent, larger studies. Funding Source - FDA OOPD.

Conditions

Cushing Disease

Study Design

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

Study Groups

Fimepinostat 60mg

two 30mg capsules once a day, 10 subjects

Group Type: ACTIVE_COMPARATOR

Fimepinostat

Intervention Type: DRUG

The study will allow us to determine the efficacy and safety of these doses in the treatment of Cushing Disease (CD) and guide dose selection for subsequent, larger studies.

Fimepinostat 30mg

single 30mg capsule daily in 10 subjects

Group Type: ACTIVE_COMPARATOR

Fimepinostat

Intervention Type: DRUG

The study will allow us to determine the efficacy and safety of these doses in the treatment of Cushing Disease (CD) and guide dose selection for subsequent, larger studies.

Interventions

Fimepinostat

The study will allow us to determine the efficacy and safety of these doses in the treatment of Cushing Disease (CD) and guide dose selection for subsequent, larger studies.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Male and female patients at least 18 years old
• Patients with confirmed pituitary origin Cushing syndrome defined as 1, 2& 3 or 4 & 5 below:

1. Persistent hypercortisolism defined as a mean of 3 consecutive 24h UFC at baseline assessment ≥ 1.3x ULN

2. Normal or elevated plasma ACTH levels

3. Pituitary adenoma > 4mm visible on MRI or inferior petrosal sinus sampling (IPSS) central to peripheral ACTH gradient >2 at baseline and/or >2 after DDAVP stimulation.

4. Recurrent or persistent CD defined as pathologically confirmed previously resected pituitary ACTH-secreting tumor, and 24 hour UFC >ULN at least 4 weeks after pituitary surgery.

5. Patients on medical treatment for CD. Washout periods will be completed as below before screening: Inhibitors of steroidogenesis (metyrapone, ketoconazole, osilodristat,

• Levo-ketoconazole): 2 weeks
• SRLs (pasireotide): 2 weeks
• Progesterone receptor antagonist (mifepristone): 2 weeks
• Dopamine agonists (cabergoline): 4 weeks
• CYP3A4 strong inducers or inhibitors: varies between drugs; minimum 5-6 times the half-life of drug

Exclusion Criteria

• Patients with compromised visual fields, or evidence of visual changes within past 6 months
• Patients with sellar tumor abutting or compressing the optic chiasm on MRI and normal visual fields
• Patients with Cushing's syndrome not due to an ACTH-secreting pituitary tumor
• Patients who have undergone major surgery including pituitary surgery within 1 month of screening or who have any major surgical procedures planned across the study period
• Patients with serum potassium < 3.5 mEq/L unless stably controlled on potassium supplementation
• Patients with poorly-controlled Diabetes mellitus evidenced by HbA1c levels >8
• Patients with poorly controlled hypertension (i.e. blood pressure ≥ 160/100 mm Hg)
• Patients who have clinically significant cardiovascular impairment, as evidenced by the presence of bradycardia, ventricular tachycardia, history of myocardial infarction within past year, or any other cardiovascular impairment that may pose significant health risk in view of the investigator.
• Patients with liver disease or history of liver disease such as cirrhosis, chronic active hepatitis B and C, or chronic persistent hepatitis, or patients with ALT or AST >1.5 x ULN, serum total bilirubin >ULN, serum albumin <0.67 x LLN at screening
• Patients with renal disease or history of renal disease with creatinine clearance of 30 cm3/min or less and/or creatinine > 1.5 mg/dl at screening
• Patients not biochemically euthyroid. Patients receiving thyroid-replacement therapy must be on a stable dose for at least 3 months.
• Patients who are known to be positive for HIV, or any other condition that significantly compromises subject's immune system.
• History of alcohol abuse or illicit substance use within past year.
• Female patients who are pregnant or lactating or are of childbearing potential unless willing to practice acceptable method of birth control. Women participating in the trial must employ double barrier method through oral contraceptive or diaphragm with partner utilizing a condom. Abstinence is an acceptable form of birth control if routinely practiced. Male participants must utilize a condom with spermicidal cap/jelly and agree to not donate sperm for up to 3 months beyond main study period.
• Patients who have participated in any clinical investigation with an investigational drug within 1 month prior to screening or within 5 half-lives of the investigational treatment whichever is longer.
• Patients with concomitant treatment of strong CYP3A4 inducers or inhibitors.
• Patients who have received pituitary irradiation within the last 5 years prior to the baseline visit
• Patients with known hepatitis B surface antigen (HbsAg) positivity
• Patients with known hepatitis C antibody (anti-HCV) positivity

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

University of California, Los Angeles

OTHER

Sponsor Role: lead

Responsible Party

Anthony P. Heaney

Professor-in-Residence, Medicine

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Ronald Reagan Medical Center

Los Angeles, California, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

Anthony Heaney, MD

Role: CONTACT

csantana@mednet.ucla.edu

310-825-5874

Cristian Santana, BS

Role: CONTACT

csantana@mednet.ucla.edu

310-825-5874

Other Identifiers

R01FD007548-01A1

Identifier Type: FDA

Identifier Source: secondary_id

View Link

FD-07548-01-A1

Identifier Type: -

Identifier Source: org_study_id