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
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]
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. | |||||
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