Sotagliflozin for Cardiotoxicity

(SPARTACUS Trial)

CG
JA
Overseen ByJuan Antonio Requena-Ibanez
Age: 18+
Sex: Any
Trial Phase: Phase 2
Sponsor: Icahn School of Medicine at Mount Sinai
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This project aims to determine the benefits of the dual SGLT1/2 inhibition as prophylactic treatment to prevent anthracycline-related cardiotoxicity.

Who Is on the Research Team?

SM

Santos-Gallego, MD

Principal Investigator

Icahn School of Medicine at Mount Sinai

CG

Carlos G Santos-Gallego, MD

Principal Investigator

Icahn School of Medicine at Mount Sinai

Are You a Good Fit for This Trial?

Inclusion Criteria

I have been newly diagnosed with lymphoma.
I am scheduled to get a high dose of anthracycline chemotherapy.
I am able to care for myself and do some daily activities.
See 1 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive either Sotagliflozin 400mg per day or a matching placebo to prevent anthracycline-related cardiotoxicity

9-10 months

Follow-up

Participants are monitored for safety and effectiveness after treatment, including assessments of cardiac function and biomarkers

1 month

What Are the Treatments Tested in This Trial?

Interventions

  • Sotagliflozin

How Is the Trial Designed?

2

Treatment groups

Active Control

Placebo Group

Group I: SotagliflozinActive Control1 Intervention
Group II: PlaceboPlacebo Group1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Icahn School of Medicine at Mount Sinai

Lead Sponsor

Trials
933
Recruited
579,000+

American Heart Association

Collaborator

Trials
352
Recruited
6,196,000+