Overview
Ispronicline is under investigation in clinical trial NCT00109564 (A Safety and Efficacy Study of Ispronicline (TC-1734-112) in Subjects With Age Associated Memory Impairment (AAMI)).
Indication
No indication information available.
Associated Conditions
No associated conditions information available.
Research Report
Ispronicline (AZD-3480): A Comprehensive Review of a Selective α4β2 Nicotinic Receptor Agonist from Clinical Promise to Discontinuation
Compound Identification and Physicochemical Properties
Ispronicline is an investigational small molecule drug developed for the treatment of cognitive and neurological disorders.[1][ Throughout its development, it has been referred to by several names and codes, which are essential for navigating the scientific and clinical literature. A comprehensive understanding of its identity and chemical properties provides the foundation for interpreting its pharmacological and clinical profile.]
Nomenclature and Regulatory Identifiers
The compound was assigned the International Nonproprietary Name (INN) and United States Adopted Name (USAN) of Ispronicline.[1] During its preclinical and clinical development phases, it was known by several developmental codes, most prominently TC-1734 (by Targacept), AZD-3480 (by AstraZeneca), and RJR-1734 (by R.J. Reynolds).[2] The IUPAC nomenclature for the molecule is (2S,4E)-5-(5-isopropoxypyridin-3-yl)-N-methylpent-4-en-2-amine, with minor variations such as (E,2S)-N-methyl-5-(5-propan-2-yloxy-3-pyridinyl)pent-4-en-2-amine also appearing in chemical databases.[2][ For unambiguous identification, a set of regulatory and database identifiers has been assigned, which are consolidated in Table 1.]
Chemical Structure and Properties
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|---|---|---|---|---|
2011/11/06 | Phase 2 | Completed | |||
2008/10/22 | Phase 1 | Terminated | |||
2008/07/11 | Phase 1 | Terminated | |||
2008/06/06 | Phase 1 | Completed | |||
2008/06/03 | Phase 1 | Completed | |||
2008/06/03 | Phase 1 | Completed | |||
2008/05/29 | Phase 1 | Completed | |||
2008/05/29 | Phase 1 | Completed | |||
2008/05/23 | Phase 2 | Completed | |||
2007/09/12 | 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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