A Study for Oral SY-2101 for Participants With Acute Promyelocytic Leukemia

Acute Promyelocytic Leukemia Clinical Trial

Official title:

An Open-label Phase 1 Study to Evaluate Pharmacokinetics, Safety, and Tolerability of SY-2101 in Adult Patients With Acute Promyelocytic Leukemia

Clinical Trial Details — Status: Suspended

Administrative data

• NCT number: NCT04996030
• Other study ID #: SY-2101-101
• Status: Suspended
• Phase: Phase 1
• Start date: September 17, 2021
• Est. completion date: April 2024

Study information

• Verified date: January 2024
• Source: Syros Pharmaceuticals
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

SY-2101 is being studied as a treatment for participants with a type of leukemia called acute promyelocytic leukemia (APL). SY-2101 is an oral formulation of a drug called arsenic trioxide (ATO). ATO is already used to treat APL in a formulation that is given as an intravenous (IV) infusion (through a needle in the arm). SY-2101 is a formulation of ATO that is taken orally (by mouth).

This trial will include participants with APL in remission, who are receiving standard of care (SOC) treatment with all-trans-retinoic acid (ATRA) and IV ATO, during the consolidation phase of chemotherapy or within the past 6 months. The participants in this trial will receive continued treatment with ATO and ATRA to help keep their cancer from coming back. There will be some weeks when participants receive IV ATO and others when they receive SY-2101 (ATO taken orally). Participants with high-risk APL may be eligible for part 1 or 4 of the study for the 6 months following completion of their standard of care ATRA and ATO treatment.

Description:

This study includes 4 parts. In the first part, enrolled participants will receive a single dose of IV ATO, followed a week later by a single dose of SY-2101, SY-2101 will be administered to participants in either a fed or a fasted condition. A week after that, participants will receive a second, a single dose of SY-2101, with some participants taking this dose in a fed state and other participants taking this dose in a fasted condition. After each of these doses, blood draws and safety assessments will be performed. In the second part, enrolled participants will receive IV ATO according to the standard of care, with collection of blood and safety assessments. In the third part, enrolled participants who are documented to be in molecular remission will receive SY-2101 in place of IV ATO during the 4th cycle of consolidation, with the collection of blood and safety assessments throughout the cycle. In the fourth part, enrolled participants will receive two single-dose treatments of SY-2101 approximately one week apart.

Recruitment information / eligibility

• Status: Suspended
• Enrollment: 16
• Est. completion date: April 2024
• Est. primary completion date: January 3, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Key Inclusion Criteria:

• Participants must have a diagnosis of APL characterized by the presence of the t(15;17) translocation or PML/RARA gene expression via reverse transcription polymerase chain reaction (RT-PCR), fluorescence in situ hybridization (FISH), or cytogenetics. Participants with low-risk APL may be eligible for all parts of this study; participants with high-risk APL are only eligible for the single-dose modules if they have completed a treatment regimen that included ATO within 6 months prior to the Screening Visit.

• Participants must have received ATO plus ATRA induction therapy and must have received or be eligible and planning to receive consolidation therapy with ATO plus ATRA in alignment with National Comprehensive Cancer Network (NCCN) guidelines for low-risk APL prior to their enrollment in the study; or participants must have completed a treatment regimen that included ATO within 6 months prior to the Screening Visit.

• Participants must be able to tolerate full dose ATO per NCCN guidelines.

• Participants must be in morphological complete remission (CR) at the end of induction.

• Participants must have a serum or high-sensitivity urine pregnancy test (for females of childbearing potential) that is negative at the Screening Visit and immediately prior to initiation of study treatment (first dose of study drug).

Key Exclusion Criteria:

• Participants who have demonstrated relapse and therefore are not eligible for further consolidation.

• Participants currently receiving treatment for a non-APL malignancy (not including basal cell carcinoma, non-melanoma skin cancer, cervical carcinoma in situ, or localized prostate cancer treated with hormone therapy). Participants with history of other cancers should be free of disease for at least 2 years prior to the Screening Visit.

• Participants with an active, life-threatening, or clinically-significant uncontrolled systemic infection requiring hospitalization.

• Immunocompromised participants with increased risk of opportunistic infections, including known human immunodeficiency virus (HIV)-positive participants with cluster of differentiation 4 (CD4) counts =350 cells/millimeters (mm^3) or history of opportunistic infection in the last 12 months.

• Participants with a known active or chronic hepatitis B or active hepatitis C virus (HCV) infection. Participants with a history of HCV infection who have completed curative therapy for HCV at least 12 weeks before the Screening Visit and have a documented undetectable viral load at the Screening Visit are eligible for enrollment.

• Participants who have not adequately recovered from a major surgery within 4 weeks of starting study drug administration.

• Participants who received any other investigational agents within 4 weeks of the Screening Visit or <5 half-lives since completion of previous investigational therapy have elapsed, whichever is shorter.

• Participants who have a hypersensitivity to arsenic.

• Participants who have experienced the following Grade =3 non-hematologic toxicities associated with ATO administration: QT prolongation, hepatotoxicity, neurotoxicity, cardiac function abnormalities. Participants who experienced other severe and life-threatening clinically-significant ATO-related AEs that are considered, in the judgement of the investigator, to increase participant risk with continued ATO treatment are also excluded.

Other inclusion/exclusion criteria may apply.

Related Conditions & MeSH terms

• Acute Promyelocytic Leukemia
• Leukemia
• Leukemia, Promyelocytic, Acute

Intervention

Drug:
• SY-2101
SY-2101 will be administered per dose and schedule specified in arm description.
• Arsenic Trioxide
IV ATO will be administered per dose and schedule specified in arm description.

Locations

Country	Name	City	State
United States	University of Michigan	Ann Arbor	Michigan
United States	John Hopkins University	Baltimore	Maryland
United States	University of Alabama at Birmingham	Birmingham	Alabama
United States	Northwestern Memorial Hospital	Chicago	Illinois
United States	University of Texas Southwestern Medical Center	Dallas	Texas
United States	The University of Texas MD Anderson Cancer Center	Houston	Texas
United States	Weill Cornell Medical College	New York	New York
United States	UPMC Hillman Cancer Center	Pittsburgh	Pennsylvania

Sponsors (1)

Lead Sponsor	Collaborator
Syros Pharmaceuticals

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Single-Dose Module: Maximum Observed Plasma Concentration (Cmax) of SY-2101		Predose and up to 168 hours postdose
Primary	Single-Dose Module: Area Under the Curve (AUC) of SY-2101		Predose and up to 168 hours postdose
Primary	Multiple-Dose Module: Cmax of SY-2101		Predose and up to 6 hours postdose on Day 5 and up to 4 hours postdose on Day 26
Primary	Multiple-Dose Module: AUC of SY-2101		Predose and up to 6 hours postdose on Day 5 and up to 4 hours postdose on Day 26
Secondary	Single-Dose Module: Cmax of ATO		Predose and up to 168 hours postdose
Secondary	Single-Dose Module: AUC of ATO		Predose and up to 168 hours postdose
Secondary	Multiple-Dose Module: Cmax of ATO		Predose and up to 6 hours postdose on Day 5 and up to 4 hours postdose on Day 26
Secondary	Multiple-Dose Module: AUC of ATO		Predose and up to 6 hours postdose on Day 5 and up to 4 hours postdose on Day 26
Secondary	Number of Participants With Adverse Events		up to Day 23 for single-dose module and up to Day 56 for multiple-dose module

External Links

•   https://aplstudy.com/