Asset profile

AJH-2947

Small molecule

Phase 1Undisclosed / early pipeline
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Earlyevidence

Evidence outlook

Early-stage evidence only

Phase 1 / first-in-human studies establish safety, tolerability, and dosing; they are not designed to demonstrate efficacy, so no evidence signal is assigned yet. The first graded signal arrives with a completed confirmatory readout.

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Competitive landscape

15 competitors in this universe: 0 direct rivals (same mechanism and indication), 0 same-class, 15 same-indication; 15 further along in development.

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DrugStageModalityMechanismEvidence signalReported efficacygraded featured trials
AJH-2947: this drugPhase 1Small molecule—
Capsaicin (Qutenza)ApprovedSmall moleculeTRPV1 (transient receptor potential vanilloid 1) channel
Duloxetine (Cymbalta)ApprovedSmall moleculeSerotonin/norepinephrine transporter, Serotonin and norepinephrine transporters (SERT/NET)
PregabalinApprovedSmall moleculeα2δ subunit of voltage-gated calcium channels
SuzetrigineApprovedSmall moleculeVoltage-gated sodium channel NaV1.8
TapentadolApprovedSmall moleculeMu-opioid receptor and norepinephrine transporter (NET)
CrisugabalinPhase 3Small moleculeα2δ-1 subunit of voltage-gated calcium channels
MirogabalinPhase 3Small moleculeα2δ-1 subunit of voltage-gated calcium channels
HL-1186Phase 2/3Small molecule—
HRS-2129Phase 2/3Small molecule—
JMKX000623Phase 2Small moleculeVoltage-gated sodium channel NaV1.8
LY4065967Phase 2Small moleculeAngiotensin II type 2 receptor (AT2R) (antagonist)
NRD135S.E1Phase 2Small molecule—
PilavapadinPhase 2Small moleculeAP2-associated kinase 1 (AAK1)
Pirenzepine (topical)Phase 2Small moleculeMuscarinic acetylcholine receptor (M3), Muscarinic M1 receptor (antagonist)
VX-993Phase 2Small moleculeVoltage-gated sodium channel NaV1.8
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Research adds each competitor's evidence grade and sourced trial results, aligned per race, so you can see who actually has the data.

Upcoming events

No upcoming readouts on record for this asset.

All registered studies

Every ClinicalTrials.gov study of this drug's own program, grouped by indication and phase. Research unlocks the studies themselves: titles, statuses, dates and featured-trial cross-links.