TheraRadar
Data updated: May 26, 2026

LOPRESSOR (metoprolol tartrate)

Trial Activity: Stable 2 active trials
Cardiovascular Approved 1978-08-07

1 IND ICATIONS AND USAGE LOPRESSOR is a beta-adrenergic blocker indicated for the treatment of: Hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. Angina Pectoris. Myocardial Infarction, to reduce the risk of cardiovascular mortality when used in conjunction with intravenous metoprolol therapy in patients with definite or suspected acute myocardial infarction in hemodynamicall...

Source: FDA Label • VALIDUS PHARMS

Development Insights

University of Chicago conducting 1 trials (20%)
7 indications explored (Moderate)
coronary arterial disease (cad) (2 trials)
heart diseases (1 trials)
ischemic heart disease (ihd) (1 trials)
7
Indications
--
Phase 3 Trials
1
Priority Reviews
47
Years on Market

Details

Status
Prescription
First Approved
1978-08-07
Routes
ORAL, INJECTION
Dosage Forms
TABLET, INJECTABLE, SOLUTION, TABLET, EXTENDED RELEASE

LOPRESSOR Approval History

1979
1980
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Original
New Indication
New Form
Label Update
155 FDA actions from 1978 to 2025 · 3 indication expansions
Nov 2025 SUPPL
Label · Labeling
Aug 2025 ORIGINAL
Update · Type 5 - New Formulation or New Manufacturer
Apr 2025 ORIGINAL
New Form · Type 3 - New Dosage Form

What LOPRESSOR Treats

7 FDA approvals

Originally approved for its first indication in 1978 . Covers 7 distinct patient populations.

  • Other (7)
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Clinical Trial Registry

5 trials
Trial Sponsor ID Phase Status Title
NCT03138603 ORION results posted IRB19-1797 5R01HL126892 Ph 3 completed Metoprolol to Reduce Perioperative Myocardial Injury
NCT07268170 HEART-BEAT 2025-522741-21-00 2025-522741-21-00 Ph 2, Ph 3 enrolling by invitation Heart Rate Control Before Cardiac Computed Tomography in Adults for the Evaluation of Coronary Artery Disease
NCT06864234 BEACON 2025/032 Ph 4 recruiting Effect of Beta-blockers on Coronary Flow and Resistance in Patients With ANOCA
NCT05008250 2013019 Ph 4 completed Efficacy and Safety of Metoprolol Tartrate Tablets Combined With Chinese Traditional Medicine on Premature Ventricular Complex.
NCT03457597 CORT125134-126 Ph 1 completed Study in Healthy Subjects to Determine the Effect of Relacorilant on Exposure to Probe Substrates for Cytochrome P450s
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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

Pro

Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

LOPRESSOR FDA Label Details

Indications & Usage

FDA Label (PDF)

1 IND ICATIONS AND USAGE LOPRESSOR is a beta-adrenergic blocker indicated for the treatment of: Hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. Angina Pectoris. Myocardial Infarction, to reduce the risk of cardiovascular mortality when used in conjunction with intravenous metoprolol therapy in patients with definite or suspected acute myocardial infarction in hemodynamically stable patients. 1.1 Hypertension LOPRESSOR is indicated for the treatment of hypertension in adul...

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.

How We Calculate These Metrics

Trial Activity Stage

Measures the current development activity pattern based on trial phases, status, and trends. Important: This measures R&D activity, not commercial lifecycle.

Trial statuses: "Active" means recruiting or ongoing. "Completed" means reached planned endpoint. "Terminated" means stopped early—often due to safety, efficacy, or business reasons.

  • Growth: High proportion of early-phase trials (Phase 1/2), active development
  • Expansion: Significant Phase 3 activity, approaching or pursuing approvals
  • Mature: Substantial Phase 4 post-marketing studies
  • Stable: Mixed phase distribution, steady development
  • Declining: Low active trial ratio, reduced R&D investment