ADENOSCAN (adenosine) · ASTELLAS
Development Insights
Details
- Status
- Discontinued
- First Approved
- 1995-05-18
- Routes
- INTRAVENOUS
- Dosage Forms
- SOLUTION
ADENOSCAN Approval History
What ADENOSCAN Treats
2 FDA approvalsOriginally approved for its first indication in 1995 . Covers 2 distinct patient populations.
- Other (2)
ASTELLAS's other novel FDA approvals
Other CDER-designated drugs from the same sponsor (2016–2025).
Clinical Trial Registry
25 trials| Trial | Sponsor ID | Phase | Status | Title |
|---|---|---|---|---|
| NCT06993038 COMFORT-ED | 202412202 | Ph 4 | recruiting | Adenosine vs Diltiazem for Treatment of SVT in the ED |
| NCT03218137 | 1609017561 | Ph 4 | recruiting | Use of Adenosine to Determine the Electrophysiological Mechanism of Premature Ventricular Contractions |
| NCT06578234 HYPER | 2023-505248-20-00 | Ph 4 | recruiting | Hyperemic mYocardial Perfusion by adEnosine at diffeRent Doses |
| NCT06717685 | PIC001/2024 | Ph 3 | recruiting | Efficacy of Adenosine as Compared to Verapamil in Paroxysmal Supraventricular Tachycardia (pSVT) Patients |
| NCT04666454 | BROKEN SWEDEHEART | Ph 4 | recruiting | BROKEN-SWEDEHEART- Optimized Pharmacological Treatment for Broken Heart (Takotsubo) Syndrome. |
| NCT03557385 ACCELERATION results posted | Pro00093001 | Ph 4 | completed | Adenosine Contrast CorrELations in Evaluating RevAscularizaTION |
| NCT05014061 A-STAMI | EudraCT number: 2021-001466-37 | Ph 3 | withdrawn | Adenosine's Effect on STunning Resolution in Acute Myocardial Infarction |
| NCT04588441 | IRB202002127 OCR39505 | Ph 2 | withdrawn | The ARCTIC Trial: Aerosolized Inhaled Adenosine Treatment in Patients With Acute Respiratory Distress Syndrome (ARDS) Caused by COVID-19 |
| NCT03236311 results posted | ACT14656 2016-000629-38, U1111-1182-1709 | Ph 2 | terminated | A Dose Titration Study to Assess the Effects of SAR407899 in Patients With MVA and/or Persistent Stable Angina Despite Angiographically Successful PCI |
| NCT04392362 AHAvsSIM results posted | UPretoria | Ph 3 | completed | A Trial to Compare American Heart Association (AHA) and Simple (SIM)Method to Give Adenosine to Treat Supra-ventricular Tachycardia (SVT) |
| NCT04699110 | ERC-76/2020 | Ph 4 | completed | Adrenaline for the Treatment of No-Reflow in Normotensive Patients |
| NCT03249272 results posted | Pro00082447 | Ph 4 | terminated | Microvascular Dysfunction in Nonischemic Cardiomyopathy: Insights From CMR Assessment of Coronary Flow Reserve |
| NCT02867878 TITAN | 160596 | Ph 2 | terminated | Adenosin to Rapidly Reverse Left Ventricle Impairment in Takotsubo Syndrome |
| NCT01690884 | 120477 | Ph 1 | completed | Effect of Ticagrelor vs. Dipyridamole on Adenosine Uptake |
| NCT02462941 | AAAO8054 | Ph 1 | completed | Analysis of Adenosine on Sinus and Atrioventricular Nodal Conduction in the Pediatric Transplanted Heart |
| NCT03032965 results posted | HUM00048922 | Ph 2 | completed | Adenosine to Assess Complete Conduction Block During Catheter Ablation of Paroxysmal Atrial Fibrillation |
| NCT03231371 CFR-OHT results posted | HUM23585 | Ph 3 | completed | Coronary Artery Vasculopathy in Pediatric Heart Transplant Patients |
| NCT01161121 results posted | Rega-9I06 | Ph 1 | completed | Comparison of Intravenous Adenosine Infusion With Regadenoson Bolus for Inducing Maximal Coronary Hyperemia |
| NCT01234870 results posted | CR1_STU00006013 ASCA-9J02 | Ph 2, Ph 3 | completed | Comprehensive Evaluation of Ischemic Heart Disease Using MRI |
| NCT01809743 | NL42049.060.12 | Ph 3 | completed | Regadenoson and Adenosine |
| NCT00781404 PROMISE | HUValldHebronRI 2007-006671-36 | Ph 3 | completed | Myocardial Protection With Adenosine During Primary Percutaneous Coronary Intervention in Pts With STEMI |
| NCT00590070 REOPEN-AMI | REOPEN-AMI 2007-006794-93 2007-006794-93 | Ph 2, Ph 3 | completed | THE REOPEN-AMI STUDY - Intracoronary Nitroprusside Versus Adenosine in Acute Myocardial Infarction |
| NCT01148147 PREVENT-ICARUS | CE 93/09 2009-013681-92 | Ph 3 | completed | Intracoronary Adenosine Administration to Prevent Periprocedural Myonecrosis in Elective Coronary Angioplasty |
| NCT01123525 | AdCard 2010 2008-004274-40 | Ph 1, Ph 2 | completed | Adenosine Cardioplegia; Improved Cardioprotection? |
| NCT00881686 | xinzangwaike0002 | Ph 1, Ph 2 | completed | Myocardial Protection With Adenosine Preconditioning |
Active Pipeline
Ongoing clinical trials by development phase
Key Completed Trials
Completed studies with published results, ranked by significance
Trial Timeline
Full development history with FDA approval milestones
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.
ADENOSCAN FDA Label Details
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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