Organisation paid for research Program year 2025 Source: CMS Open Payments

Covenant Metabolic Specialists LLC

Neither a doctor nor a teaching hospital

Research payments

$1,711,117

539 payments

Through program year 2025, Covenant Metabolic Specialists LLC is reported as receiving $1,711,117 in research payments, across 539 payments.

By program year

3 rows
Year Kind Amount Payments
2025 Research $1,366,346 454
2024 Research $235,426 67
2023 Research $109,345 18

Breakdown

Who paid Research payments · program years 2023–2025
  1. Madrigal Pharmaceuticals $1,402,941 407 payments
  2. Gilead Sciences, Inc. $186,111 104 payments
  3. Takeda Pharmaceuticals U.S.A., Inc. $117,960 26 payments
  4. Genentech, Inc. $4,106 2 payments
Studies the money was for Research payments · program years 2023–2025
  1. A Phase 3 Multinational Doubleblind Randomized Placebocontrolled Study of Mgl3196 Resmetirom in Patients With Nonalcoholic Steatohepatitis Nash and Fibrosis to Resolve Nash and Reduce Progression to Cirrhosis Andor Hepatic Decompensation $869,484 214 payments
  2. A 52-Week, Phase 3, Open-Label Extension Study, With a Double-blind Lead-in, to Evaluate Safety and Biomarkers of Resmetirom (MGL-3196) in Patients With Non-alcoholic Fatty Liver Disease (NAFLD), MAESTRO-NAFLD-Open-Label-Extension (MAESTRO-NAFLD-OLE) $340,652 105 payments
  3. A 52Week Phase 3 Openlabel Extension Study With A Doubleblind Leadin to Evaluate Safety and Biomarkers of Resmetirom Mgl3196 in Patients With Nonalcoholic Fatty Liver Disease Nafld Maestronafldopenlabelextension Maestronafldole $192,804 88 payments
  4. A Multicenter, Single-arm, Open-label, Phase 1b Study to Explore the Mechanism of Action and Evaluate the Safety of Ontamalimab in Participants With Nonalcoholic Steatohepatiti s With Fibrosis Stages 2 Through 4 $105,239 16 payments
  5. The study explores the Mechanism of Action and Evaluates the Safety of Ontamalimab in Participants with Nonalcoholic Steatohepatitis with Fibrosis Stages 2 through 4 $12,721 10 payments
  6. A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Effect of Seladelpar on Clinical Outcomes in Patients With Primary Biliary Cholangitis (PBC) and Compensated Cirrhosis $11,500 1 payment
  7. A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Effect of Seladelpar on Clinical Outcomes in Patients With Primary Biliary Cholangitis (PBC) and Compensated Cirrhosis $11,500 1 payment
  8. A 52-week, Double-blind, Placebo-controlled, Randomized, Phase 3 Study Intended to Determine the Effects of Seladelpar on Normalization of Alkaline Phosphatase Levels in Subjects With Primary Biliary Cholangitis (PBC) and an Incomplete Response or Intolerance to Ursodeoxycholic Acid (UDCA) $11,050 1 payment
  9. A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Effect of Seladelpar on Clinical Outcomes in Patients With Primary Biliary Cholangitis (PBC) and Compensated Cirrhosis $10,039 1 payment
  10. An Open Label Long-Term Study to Evaluate the Safety and Tolerability of Seladelpar in Subjects With Primary Biliary Cholangitis (PBC) $9,500 1 payment

What you are looking at

A noncovered recipient is an organisation paid for research that is neither an individual clinician nor a teaching hospital — typically a contract research organisation, a foundation or a trial site network. They receive 81% of all reported research money, which is why they appear here at all.

Provenance

Source: CMS Open Payments · through program year 2025

We reproduce what manufacturers reported. We do not verify, edit or correct the underlying records.

A payment record is not evidence of wrongdoing. Financial relationships between industry and medicine are legal, common and often necessary for research. Who Paid My Doc reports what was disclosed; it does not judge it.

Who Paid My Doc is independent and is not affiliated with, endorsed by or sponsored by CMS or any U.S. government agency. It is not a consumer reporting agency and this is not a consumer report; do not use it for decisions covered by the Fair Credit Reporting Act.

How to dispute or correct a record