INREBIC

Drug Celgene Corporation
Total Payments
$3.0M
Transactions
2,028
Doctors
1,092
Companies
2

Payment Trends by Year

Year Amount Transactions Doctors
2024 $476,762 8 5
2023 $59,914 15 5
2022 $166,067 66 14
2021 $617,415 271 170
2020 $1.7M 1,668 958

Payments by Nature

Nature of Payment Amount Transactions Share
Unspecified $2.3M 104 74.3%
Compensation for services other than consulting, including serving as faculty or as a speaker at a venue other than a continuing education program $443,582 165 14.6%
Consulting Fee $151,032 75 5.0%
Travel and Lodging $90,438 127 3.0%
Food and Beverage $45,739 1,495 1.5%
Education $27,545 60 0.9%
Grant $12,500 1 0.4%
Charitable Contribution $10,000 1 0.3%

Payments by Type

Research
$2.3M
104 transactions
General
$780,836
1,924 transactions

Research Studies & Clinical Trials

Study Name Sponsor Amount Doctors
A Phase 3b, Multicenter, Single-Arm, Open-Label Efficacy & Safety Study of Fedratinib in Subjects w/ DIPSS-Intermediate or High-Risk PMF, post-PV MF, or post-ET MF & Previously Treated w/ Ruxolitinib incl. Sub-study w/ concomitant Luspatercept for anemia Celgene Corporation $598,693 0
A phase 2 study of fedratinib in myelodysplastic/myeloproliferative neoplasms (MDS/MPNs) and chronic neutrophilic leukemia (CNL) Celgene Corporation $383,181 0
A Phase 3b, Multicenter, Single-Arm, Open-Label Ef Celgene Corporation $320,497 0
A Phase 1, Open-Label, Single Dose Study to Assess the Pharmacokinetics, Safety, and Tolerability of Fedratinib in Subjects with Moderate and Severe Hepatic Impairment Compared with Healthy Subjects (BMS Study Number: CA054-P06) Celgene Corporation $276,972 0
A Phase 1 Open-label, Single-dose Study to Assess Celgene Corporation $241,114 0
(FEDR-CP-002 (PMC)) A Phase 1, Open-label, 2-part Study to Evaluate the Effect of Rifampin and Efavirenz on the Pharmacokinetics of Fedratinib in Healthy Adult Subjects (BMS Study Number: CA054-P07) Celgene Corporation $179,184 0
A Phase 3b, Multicenter, Single-Arm, Open-Label Ef - A Phase 3b, Multicenter, Single-Arm, Open-Label Efficacy and Safety Study of Fedratinib in Subjects with DIPSS (Dynamic International Prognostic Scoring System)-Intermediate or High-Risk Primary Myelofi Celgene Corporation $89,838 0
Phase I Trial of Fedratinib in Combination with Decitabine in Patients with Myeloproliferative Neoplasms in Accelerated and Blast Phase Celgene Corporation $72,736 0
A Phase 1 Open-label, Single-dose Study to Assess - A Phase 1 Open-label, Single-dose Study to Assess the Pharmacokinetics, Safety, and Tolerability of Fedratinib in Subjects with Moderate and Severe Hepatic Impairment Compared with Healthy Subjects Celgene Corporation $30,512 0
A Phase 1, Open-Label, Single Dose Study to Assess the Pharmacokinetics, Safety, and Tolerability of Fedratinib in Subjects with Moderate and Severe Hepatic Impairment Compared with Healthy Subjects Celgene Corporation $26,060 0
(FEDR-CP-005) BE Study - A Phase 1, Open-label, Single-center, 2-part Crossover Study to Evaluate the Relative Bioavailability of Fedratinib When Administered as Contents of Capsules Dispersed in a Nutritional Supplement Orally or Via Nasogastric Tube, or Celgene Corporation $24,689 0
A Phase I/II GVHD Prevention trial combining fedratinib with sirolimus and post-transplant cyclophosphamide for allogeneic HLA matched donor using peripheral blood stem cells. Celgene Corporation $16,032 0
A Phase 1/2, Multicenter, Single-arm, Open-label Study to Evaluate the Efficacy and Safety of Fedratinib in Japanese Subjects With DIPSS (Dynamic International Prognostic Scoring System) E.R. Squibb & Sons, L.L.C. $2,160 2
A Phase I/II Trial of Maintenance Fedratinib to Prevent Post-Transplant Relapse in Myeloproliferative Neoplasms Celgene Corporation $768.00 0
A Phase 3b, Multicenter, Single-Arm, Open-Label Ef - A Phase 3b, Multicenter, Single-Arm, Open-Label Efficacy and Safety Study of Fedratinib in Subjects with DIPSS (Dynamic International Prognostic Scoring System)-Intermediate or High-Risk Primary Myelofibrosis Celgene Corporation $590.00 0
A Phase 1, Open-label Study to Evaluate the Influence of Fedratinib on the Pharmacokinetics of Transporter Probe Substrates (Digoxin, Rosuvastatin, and Metformin) in Healthy Adult Subjects Celgene Corporation $122.22 0

Top Doctors Receiving Payments for INREBIC

Doctor Specialty Location Total Records
Irene Hutchins La Quinta, CA $2.3M 107
, M.D Medical Oncology Bethesda, MD $82,951 28
, MD Hematology & Oncology Jersey City, NJ $57,114 39
Bart Scott Medical Oncology Seattle, WA $47,930 28
, MD Hematology & Oncology Minneapolis, MN $35,656 26
, MD Hematology & Oncology New Orleans, LA $32,019 21
, MD Medical Oncology Orange, CA $24,309 15
, MD Hematology & Oncology San Antonio, TX $23,888 8
, MD Internal Medicine Orlando, FL $21,803 14
, MD Internal Medicine Ann Arbor, MI $21,758 7
, MD Medical Oncology Dallas, TX $21,028 10
, MD Hematology & Oncology San Diego, CA $18,349 10
, MD Internal Medicine Stony Brook, NY $16,767 11
, M.D Internal Medicine Duarte, CA $16,089 17
, M.D Hematology & Oncology Carmel, IN $14,762 16
, M.D Internal Medicine Gardena, CA $14,173 8
, M.D Internal Medicine Tampa, FL $13,857 7
, M.D Hematology & Oncology Memphis, TN $12,569 10
, M.D Specialist Columbia, MD $11,744 6
, M.D Hematology & Oncology Birmingham, AL $11,359 7
, M.D Hematology Hawthorne, NY $11,274 7
, MD Hematology & Oncology Atlanta, GA $11,077 8
, M.D Hematology & Oncology Omaha, NE $11,027 7
, MD Hematology & Oncology Orlando, FL $10,933 11
, MD Hematology & Oncology New York, NY $10,915 4

About INREBIC

INREBIC is a drug associated with $3.0M in payments to 1,092 healthcare providers, recorded across 2,028 transactions in the CMS Open Payments database. The primary manufacturer is Celgene Corporation.

Payment data is available from 2020 to 2024. In 2024, $476,762 was paid across 8 transactions to 5 doctors.

The most common payment nature for INREBIC is "Unspecified" ($2.3M, 74.3% of total).

INREBIC is associated with 16 research studies, including "A Phase 3b, Multicenter, Single-Arm, Open-Label Efficacy & Safety Study of Fedratinib in Subjects w/ DIPSS-Intermediate or High-Risk PMF, post-PV MF, or post-ET MF & Previously Treated w/ Ruxolitinib incl. Sub-study w/ concomitant Luspatercept for anemia" ($598,693).