Synribo

Drug Teva Pharmaceuticals USA, Inc.
Total Payments
$1.1M
Transactions
40
Doctors
0
Companies
1

Payment Trends by Year

Year Amount Transactions Doctors
2024 $66,545 2 0
2023 $299,453 9 0
2022 $408,744 13 0
2021 $123,429 5 0
2020 $169,392 5 0
2018 $80,036 6 0

Payments by Nature

Nature of Payment Amount Transactions Share
Unspecified $1.1M 40 100.0%

Research Studies & Clinical Trials

Study Name Sponsor Amount Doctors
Phase Ib/II study of omacetaxine and venetoclax for patients with relapsed/refractory acute myeloid leukemia or myelodysplastic syndrome harboring mutant RUNX1 Teva Pharmaceuticals USA, Inc. $358,320 0
VEN-OM: Phase IB/II Study Of Safety And Efficacy Of Venetoclax When Combined With Escalating Doses Of Omacetaxine In Patients With Relapsed/Refractory Hematologic Malignancies Failing Treatment With Venetoclax-Containing Regimens Teva Pharmaceuticals USA, Inc. $207,224 0
Patient-centered approach to elicit and compare the treatment goals of patients with episodic and chronic migraine and healthcare providers Teva Pharmaceuticals USA, Inc. $150,754 0
A Phase II Study of Omacetaxine (OM) in Patients with Intermediate-1 and Higher Risk Myelodysplastic Syndrome (MDS) post Hypomethylating Agent (HMA) Failure Teva Pharmaceuticals USA, Inc. $96,000 0
Concomitant Omacetaxine Mepesuccinate and Azacitidine for Patients with Previously Untreated High Grade Myelodysplastic Syndromes Teva Pharmaceuticals USA, Inc. $83,065 0
VEN-OM: Phase IB/II Study Of Safety And Efficacy Of Venetoclax When Combined With Escalating Doses Of Omacetaxine In Patients With Relapsed/Refractory Hematologic Malignancies Failing Treatment With Venetoclax-Containing Regimens _ Teva Pharmaceuticals USA, Inc. $56,604 0
Omacetaxine Mepesuccinate with Azacitidine for Patients with Previously Untreated Higher Risk Myelodysplastic Syndrome Teva Pharmaceuticals USA, Inc. $48,928 0
A Phase II Study of Omacetaxine (OM) in Patients With Intermediate-1 and Higher Risk Myelodysplastic Syndrome (MDS) Post Hypomethylating Agent (HMA) Failure Teva Pharmaceuticals USA, Inc. $46,349 0
Studies to determine the pre-clinical in vivo efficacy of Omecetaxine against human AML xenograft expressing mutant RUNX1. Teva Pharmaceuticals USA, Inc. $33,360 0
Patient-centered approach to elicit and compare the treatment goals of patients with episodic and chronic migraine and healthcare providers_ Teva Pharmaceuticals USA, Inc. $33,308 0
Phase IB/II Study of Omacetaxine with Cytarabine and Idarubicin Induction Therapy for Patients with de novo Acute Myelogenous leukemia Teva Pharmaceuticals USA, Inc. $29,046 0
An Open-Label, Single-Group Clinical Study to Evaluate the Pharmacokinetics, Safety,and Efficacy of Omacetaxine Mepesuccinate Given Subcutaneously as a Fixed Dose inPatients With Chronic Phase or Accelerated Phase Chronic Myeloid Leukemia Who Have Failed 2 or More Tyrosine Kinase Inhibitor Therapies Teva Pharmaceuticals USA, Inc. $4,641 0

Top Doctors Receiving Payments for Synribo

Doctor Specialty Location Total Records
Unknown Chicago, IL $1.1M 40

About Synribo

Synribo is a drug associated with $1.1M in payments to 0 healthcare providers, recorded across 40 transactions in the CMS Open Payments database. The primary manufacturer is Teva Pharmaceuticals USA, Inc..

Payment data is available from 2018 to 2024. In 2024, $66,545 was paid across 2 transactions to 0 doctors.

The most common payment nature for Synribo is "Unspecified" ($1.1M, 100.0% of total).

Synribo is associated with 12 research studies, including "Phase Ib/II study of omacetaxine and venetoclax for patients with relapsed/refractory acute myeloid leukemia or myelodysplastic syndrome harboring mutant RUNX1" ($358,320).