ACY 241 in Combination With Paclitaxel in Patients With Advanced Solid Tumors

Advanced Solid Tumors Clinical Trial

Official title:

A Phase 1b Study of the Safety, Pharmacokinetics, and Preliminary Antitumor Activity of ACY 241 in Combination With Paclitaxel in Patients With Advanced Solid Tumors

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02551185
• Other study ID #: ACE-ST-201
• Status: Completed
• Phase: Phase 1
• Start date: December 22, 2015
• Est. completion date: October 4, 2019

Study information

• Verified date: February 2020
• Source: Celgene
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a Phase 1b, multicenter, single arm, open label, dose escalation study to determine the MTD and evaluate the safety and preliminary antitumor activity of orally (PO) administered ACY 241 in combination with intravenously (IV) administered paclitaxel in eligible patients with advanced solid tumors.

Description:

Patients will receive ACY 241 with dose escalation according to a 3 + 3 design in combination with paclitaxel at the dose and schedule used in clinical practice for the patient population treated in this protocol.

Patients will undergo screening assessments for protocol eligibility within 28 days of study start (Cycle 1 Day 1).

Patients will receive ACY 241 by oral administration once daily (QD) or, if supported by PK and safety data, twice daily on 21 consecutive days of a 28 day treatment cycle. Paclitaxel will be administered to patients at 80 mg/m2 IV over 1 hour on Days 1, 8, and 15 of the 28 day treatment cycle. Patients who experience a DLT or other unacceptable toxicity in Cycle 1 will be removed from study treatment. Patients will receive study treatment until documented progressive disease (PD) or unacceptable toxicity.

Each cohort will consist of at least 3 patients. Patients who withdraw consent in Cycle 1 will be replaced. An assessment of safety will be made by the Safety Review Committee (SRC) before dose escalation. The SRC will be composed of the Study Investigators, the Sponsor's Medical Monitor and Clinical Project Lead, and the Contract Research Organization's Safety Monitor, Project Manager, and Biometrician. Ad hoc members may be invited by the Sponsor as needed.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: October 4, 2019
• Est. primary completion date: September 30, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Must be able to understand and voluntarily sign an informed consent form (ICF).

2. Must be = 18 years of age at the time of signing the ICF.

3. Must be able to adhere to the study visit schedule and other protocol requirements.

4. Patients must have a histologically confirmed nonhematological, metastatic or locally advanced, incurable malignancy for which paclitaxel is clinically appropriate. Patients must have received and failed standard treatment for their malignancy; patients for whom no standard treatment is available will also be eligible.

5. Evaluable disease by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1.

6. Life expectancy > 12 weeks.

7. Must have Eastern Cooperative Oncology Group (ECOG) performance status score of 0, 1, or 2.

8. Patients with the potential for pregnancy or impregnating their partner must agree to follow acceptable birth control methods to avoid conception. Females of childbearing potential must have a negative pregnancy test. It is not known if the antideacetylase activity of this experimental drug may be harmful to the developing fetus or nursing infant.

Exclusion Criteria:

1. Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the patient from giving informed consent.

2. Any serious concurrent medical conditions, laboratory abnormality, or psychiatric illness that might make the patient nonevaluable, put the patient's safety at risk, or prevent the patient from following the study requirements.

3. Pregnant or lactating females.

4. Patients with uncontrolled brain metastases.

5. Patients who have had chemotherapy or radiotherapy within 2 weeks (6 weeks for nitrosoureas or mitomycin C) before entering the study or those who have not recovered from AEs to = Grade 1 (except for peripheral neuropathy; see Exclusion Criterion 12) due to agents administered more than 4 weeks earlier.

6. Previous therapy with histone deacetylase (HDAC) inhibitor.

7. Any of the following laboratory abnormalities:

• ANC < 1,500/µL.

• Platelet count < 100,000/µL

• Hematologic growth factors are not allowed at Screening or during the first cycle of treatment.

• Hemoglobin < 9 g/dL (< 5.5 mmol/L; previous red blood cell [RBC] transfusion is permitted).

• Creatinine > 1.5 × upper limit of normal (ULN).

• AST or ALT > 2.5 × ULN. For patients with liver metastasis AST or ALT > 5 × ULN.

• Serum total bilirubin > 1.5 mg/dL or > 3 × ULN for patients with hereditary benign hyperbilirubinemia

8. Corrected QT interval (QTc) using Fridericia's formula (QTcF) value > 480 msec at Screening; family or personal history of long QTc syndrome or ventricular arrhythmias including ventricular bigeminy at Screening; previous history of drug induced QTc prolongation or the need for treatment with medications known or suspected of producing prolonged QTc intervals on electrocardiogram (ECG).

9. Congestive heart failure (New York Heart Association Class III or IV), myocardial infarction within 12 months before starting study treatment, or unstable or poorly controlled angina pectoris, including Prinzmetal variant angina pectoris.

10. Positive human immunodeficiency virus, hepatitis B virus, and hepatitis C virus infection.

11. Hypersensitivity to taxanes (such as Steven Johnson syndrome). Hypersensitivity, such as rash < Grade 3 that is managed, is allowed.

12. Peripheral neuropathy > Grade 2 despite supportive therapy.

13. Patients who received any of the following within the 14 days before initiating study treatment:

• Major surgery

• Radiation therapy

• Systemic therapy (standard or an investigational or biological anticancer agent)

14. Current enrollment in another clinical study involving treatment and/or is receiving an investigational agent for any reason, or use of any investigational agents within 28 days or 5 half lives (whichever is longer) of initiating study treatment.

15. Incidence of gastrointestinal disease that may significantly alter the absorption of ACY 241.

Related Conditions & MeSH terms

• Advanced Solid Tumors
• Neoplasms

Intervention

Drug:
• ACY-241

Locations

Country	Name	City	State
United States	Remove - Emory University Winship Cancer Institute	Atlanta	Georgia
United States	Beth Israel Deaconess Medical Center	Boston	Massachusetts
United States	Dana Farber Cancer Institute	Boston	Massachusetts
United States	Massachusetts General Hospital	Boston	Massachusetts
United States	CTRC at The UT Health Science Center at San Antonio	San Antonio	Texas
United States	Pinnacle Oncology Hematology	Scottsdale	Arizona

Sponsors (1)

Lead Sponsor	Collaborator
Celgene

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Dose limiting toxicities (DLTs)		12 months
Primary	Recommended phase 2 dose and schedule of ACY 241 in combination with paclitaxel on a weekly schedule.		12 months
Primary	Maximum tolerated dose (MTD), if present.		12 months
Secondary	Safety profile of ACY 241 administered in combination with paclitaxel.		12 months
Secondary	Preliminary antitumor activity of ACY 241 administered in combination with paclitaxel in the patient population.		12 months