MedPath

Mericitabine

Generic Name
Mericitabine
Drug Type
Small Molecule
Chemical Formula
C18H26FN3O6
CAS Number
940908-79-2
Unique Ingredient Identifier
TA63JX8X52

Overview

Mericitabine has been investigated for the treatment of Hepatitis C, Chronic. Mericitabine is a polymerase inhibitor being developed for the treatment of chronic hepatitis C. Mericitabine is a prodrug of PSI-6130, which demonstrated excellent potency in preclinical studies. PSI-6130 is a pyrimidine nucleoside analog inhibitor of HCV RNA polymerase, an enzyme that is necessary for hepatitis C viral replication.

Indication

No indication information available.

Associated Conditions

No associated conditions information available.

Research Report

Published: Oct 13, 2025

Diamorphine (Diacetylmorphine): A Comprehensive Pharmacological and Clinical Monograph

Introduction

Overview and Significance

Diamorphine, also known as diacetylmorphine, is a potent semi-synthetic opioid analgesic derived from morphine, the principal alkaloid of the opium poppy (Papaver somniferum L.).[1] It occupies a unique and highly contentious position in the global pharmacopoeia, defined by a profound paradox. In certain jurisdictions, most notably the United Kingdom, diamorphine is a legally prescribed, highly valued medication for managing severe pain and treating refractory opioid use disorder.[1] Conversely, in most of the world, it is known exclusively by its illicit name, heroin, a substance synonymous with addiction, societal harm, and a high potential for fatal overdose.[1] This dual identity is not merely a matter of nomenclature; it reflects a deep and long-standing international schism in medical philosophy, public health policy, and the legislative control of psychoactive substances. The drug serves as a powerful case study in how the same chemical entity can be perceived and regulated in dramatically different ways, with its value and risks being shaped as much by its socio-legal context as by its intrinsic pharmacology.

Historical Context

The history of diamorphine is intertwined with the search for more effective and safer analgesics. It was first synthesized in 1874 by C.R. Alder Wright, a chemist at St. Mary's Hospital Medical School in London, through the acetylation of morphine.[1] However, it remained a scientific curiosity until 1898, when the German pharmaceutical company Bayer began to commercially market it under the trade name "Heroin".[6] It was promoted as a powerful cough suppressant and, with a tragic lack of foresight, as a non-addictive alternative to morphine.[6] The name itself was derived from the German word heroisch ("heroic") to describe its perceived powerful effects.[6]

Continue reading the full research report

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2012/06/26
Phase 2
Completed
2012/04/17
Phase 2
Withdrawn
2011/12/01
Phase 2
Completed
2011/11/30
Phase 2
Completed
2011/11/30
Phase 2
Completed
2011/04/08
Phase 2
Completed
2011/01/17
Phase 2
Completed
2010/06/29
Phase 1
Completed
2010/04/08
Phase 1
Completed
2010/01/27
Phase 2
Completed

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
No FDA approvals found for this drug.

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
No TGA approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
No Health Canada approvals found for this drug.

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

Help Us Improve

Your feedback helps us provide better drug information and insights.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.