Komori
Occurring Fact4591RIBOMIC Inc.Pharmaceuticals

Notice of the enrollment of the first patient in the Japanese Phase III clinical trial of the achondroplasia treatment ume­daptanib pegol

RIBOMIC Inc. completed enrollment of the first patient in a domestic Phase 3 clinical trial of umedaptanib pegol for achondroplasia. Enrollment will now proceed at multiple sites in Japan, but this will have no impact on full-year results for the fiscal year ending March 2027.

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First Patient Enrollment in the Domestic Phase 3 Clinical Trial of the Achondroplasia Treatment umedaptanib pegol

Subject Entity

RIBOMIC Inc. (filing company)

Target Locations / Products

umedaptanib pegol (RBM-007), and a domestic Phase 3 clinical trial targeting pediatric patients with achondroplasia aged 2 to 14

This disclosure07/02/2026
Amount of Impact on Business Performance

No amount is specified (there will be no impact on full-year results for the fiscal year ending March 2027)

Impact on Earnings Forecast

There will be no impact on full-year earnings for the fiscal year ending March 2027

Outlook

RIBOMIC Inc. will accelerate patient enrollment at multiple sites in Japan, proceed with evaluating the treatment's clinical value, and further advance efforts toward the development of pharmaceuticals originating in Japan.

Event that occurred
ItemDetails
Event nameFirst Patient Enrollment in the Domestic Phase 3 Clinical Trial of the Achondroplasia Treatment umedaptanib pegol
Subject EntityRIBOMIC Inc. (filing company)
Target Locations / Productsumedaptanib pegol (RBM-007), and a domestic Phase 3 clinical trial targeting pediatric patients with achondroplasia aged 2 to 14
Amount of Impact on Business PerformanceNo amount is specified (there will be no impact on full-year results for the fiscal year ending March 2027)
Impact on Earnings ForecastThere will be no impact on full-year earnings for the fiscal year ending March 2027
OutlookRIBOMIC Inc. will accelerate patient enrollment at multiple sites in Japan, proceed with evaluating the treatment's clinical value, and further advance efforts toward the development of pharmaceuticals originating in Japan.
Items this document does not state (19)
Date of occurrenceDate recognized / date notice receivedCauseAccounting period in which recognizedType of litigation or proceedingCourt or authorityPlaintiffDefendantDate of filing / date of actionClaim amount / surcharge amountAmount of receivables at risk of non-collection or delayed collectionSuspended operationsScheduled resumption dateInvestigation structureMeasures to prevent recurrenceDirectors' and officers' liabilityVoting rights ownership percentage before the changeVoting rights ownership percentage after the changePlanned follow-up disclosure

These are items the company does not state in this document. We do not leave them blank, nor fill them in from other sources or by inference.

The reasons the company gives

The company's own explanation, not something inferred from the numbers.

The enrollment of the first patient is considered an important milestone demonstrating steady progress in the development pipeline. RIBOMIC Inc. will accelerate patient enrollment at multiple sites in Japan and proceed with evaluating the treatment's clinical value.

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Notice of the enrollment of the first patient in the Japanese Phase III clinical trial of the achondroplasia treatment ume­daptanib pegol | RIBOMIC Inc. (4591) timely disclosure | Komori