Overview
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Research Report
Report on Investigational Agent JNJ-89495120 (PIPE-307)
1. Introduction and Overview of JNJ-89495120 (PIPE-307)
1.1. Identification
JNJ-89495120 is an investigational, orally administered small molecule drug.[1] This compound is also prominently known in scientific literature and early development communications as PIPE-307.[1] Additional synonyms used include JNJ 89495120 and JNJ89495120.[6] The consistent use of these identifiers is important for accurately tracking the compound's development progress across different research groups and publications.
JNJ-89495120 (PIPE-307) is classified as a selective M1 muscarinic acetylcholine receptor (M1R) antagonist.[4] The M1R is one of five subtypes of muscarinic acetylcholine receptors (M1-M5), which are G-protein coupled receptors (GPCRs). M1Rs are predominantly expressed within the central nervous system (CNS), particularly in regions like the telencephalon, and are also found in autonomic ganglia. They play a significant role in mediating cholinergic neurotransmission and are implicated in various cognitive functions, including learning, memory, and attention, as well as modulating cellular responses through signaling pathways such as phospholipase C activation and the regulation of intracellular calcium levels.[8] The therapeutic strategy for PIPE-307 centers on its selective antagonism of this specific receptor subtype. For the indication of Relapsing-Remitting Multiple Sclerosis (RRMS), it is being investigated as a potentially first-in-class M1 receptor antagonist with a novel mechanism focused on remyelination.[10]
1.2. Developers and Collaborations
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2025/01/20 | Phase 2 | Recruiting |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
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No FDA approvals found for this drug. |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
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No EMA approvals found for this drug. |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
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No HSA approvals found for this drug. |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
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No NMPA approvals found for this drug. |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
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No PPB approvals found for this drug. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
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No TGA approvals found for this drug. |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
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No Health Canada approvals found for this drug. |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
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No CIMA AEMPS (Spain) approvals found for this drug. |
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
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No Philippines FDA approvals found for this drug. |
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
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No Saudi SFDA approvals found for this drug. |
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
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No Malaysia NPRA approvals found for this drug. |
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
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No UK EMC drug information found for this drug. |
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