Clinical Trials

Several clinical trials evaluate the application and observational outcomes of prasugrel in patients with acute coronary syndrome, acute myocardial infarction, heart failure, and concurrent type 2 diabetes. Sponsored by diverse academic and healthcare entities—including University Hospital Heidelberg, AstraZeneca, Tabula Rasa HealthCare, and Chiesi Farmaceutici S.p.A.—the portfolio includes both completed observational registries and actively recruiting trials. Although formal trial phases are unspecified, these studies examine real-world eligibility, comparative antiplatelet regimens, and treatment outcomes in patients undergoing percutaneous coronary intervention.

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT05774431 Recruiting
Acute Myocardial Infarction
University Hospital Heidelberg|AstraZeneca
2023-03-13 --
NCT05053828 Completed
Type2 Diabetes|Antiplatelet Drugs|Myocardial Infarction|Heart Failure
Tabula Rasa HealthCare
2021-09-20 --
NCT04471870 Completed
Acute Coronary Syndrome
Chiesi Farmaceutici S.p.A.
2020-10-23 --

(data from https://clinicaltrials.gov, updated on 2024-05-22)

Check the Prasugrel product page for in-depth specifications, including solubility, stock solutions, MOA, and working concentrations.

Compliance for Clinical Use

Mechanism and Biochemical Profile

Prasugrel irreversibly binds to the thienopyridine ADP receptor (P2Y12) on platelets, thereby blocking ADP-induced purinergic signaling and inhibiting intracellular activation cascades. This potent blockade suppresses platelet aggregation and thrombus formation, providing significant clinical efficacy in mitigating thrombotic cardiovascular events in patients with acute coronary syndrome and myocardial infarction.

Appendix RUO and cGMP Quality Standards

Quality Dimension RUO (Research Use Only) cGMP (Current Good Manufacturing Practice)
Clinical Applicability Prohibited in human clinical trials or medical diagnostics. Mandatory for human clinical trials (Phase I–III) and therapies.
Regulatory Status Non-regulated grade; exempt from drug manufacturing laws. Legally enforced by health authorities (e.g., FDA, EMA, NMPA).
Facility Environment Unclassified analytical or research laboratories. Validated Cleanrooms (ISO Class 5–8) with continuous monitoring.
Quality Control Basic purity and activity testing. Rigorous safety release testing (Sterility, Endotoxin, Mycoplasma).
Process Validation Basic equipment calibration; no process validation required. Full qualification (IQ/OQ/PQ) and complete batch records.
Quality Assurance Vendor self-declared without required formal QMS. Mandatory QA/QC unit, Change Control, CAPA, and vendor audits.
Regulatory Impact High risk of IND rejection if used as a critical raw material. Required for IND/NDA filings, supported by Drug Master Files (DMF).

Footnotes

Regulatory Note: Governed by FDA (21 CFR Parts 210/211/312), EMA (EudraLex Vol 4), ICH Guidelines (E6/Q7/Q9/Q10), and compendial standards (USP <71>/<85>/<1043>).

Note: Technical data last updated: Sep 1, 2026.