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Floatz Rating
B57/100
Confidence
Indicative
v0.2
Sponsor
AlgoRx Pharmaceuticals
Modality
UNKNOWN
Development Phase
Phase 2
Status
Dormant
Evidence ledger · v0.2

Clinical Evidence

Clinical track record: trial progression, reported outcomes, safety signals, and endpoint quality.
42Moderate confidence
Detailed axis rationale is planned and will be published soon.
TrialPhaseStatusNPrimary endpointReadout
ALGRX 4975 in the Treatment of Patients With Morton's Neuroma
Completed

Competitive Position

Competitive setting: how crowded the indication is, class-level failures, and timing against rivals.
95Moderate confidence
Detailed axis rationale is planned and will be published soon.

Same indication · Neuroma

AssetSponsorPhaseRating
Algrx 4975 (this asset)AlgoRx PharmaceuticalsP2B · 57
Onabotulinum Toxin Type-ASouthern Illinois UniversityP2CCC
LidocaineDanish Pain Research CenterN/AD
Autologous Conditioned PlasmaUkrainian Society of Regional Anesthesia and Pain TherapyN/AD

Scientific Foundation

Strength of the underlying biology: target validation, tractability, modality fit, and how related mechanisms have fared.
NR

Planned for methodology v0.2.

Development Feasibility

How realistically the program can be executed, drawing on modality precedent, enrollment dynamics, and sponsor delivery.
NR

Planned for methodology v0.2.

Commercial Opportunity

Commercial prize: addressable population, unmet need, and the value case for the indication.
NR

Planned for methodology v0.2.

IP & Exclusivity

Exclusivity position, covering patent protection and freedom-to-operate runway.
NR

Planned for methodology v0.2.

Manufacturing & Supply

Manufacturing and supply readiness, driven by modality process and scale-up risk.
NR

Planned for methodology v0.2.

Related assets

Citation

Floatz Terminal. Algrx 4975 in Neuroma. Methodology v0.2.
Rated under v0.2 effective July 8, 2026. Last refreshed July 8, 2026.
Accessed July 14, 2026.
https://terminal.floatz.ai/assets/algrx-4975-neuroma

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