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Other Disclosures4591RIBOMIC Inc.Pharmaceuticals

Report on the International Skeletal Dysplasia Society Conference

At the International Skeletal Dysplasia Society conference held in Canada, the results of the Phase 2 clinical trial of the Company's achondroplasia drug candidate umedaptanib pegol were presented and discussed. The company also noted the possibility that the ongoing Phase 3 trial could achieve an annual height-growth velocity exceeding that of existing treatments.

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Announced details

umedaptanib pegol (anti-FGF2 aptamer)
Applicable field (uses covered by this announcement)

Treatment of achondroplasia (ACH)

What the company reported numerically
Quantitative Effects

The annual height-growth velocity of competing drugs is no more than +1.7 cm. If the Company's drug achieves an annual growth velocity of +2 to +3 cm or more in the Phase 3 trial, it could become a treatment option offering significant benefit.

Relationship between the counterparty and the company
RIBOMIC Inc.4591
Relationship with the Company

The Company presented and discussed the results of its Phase 2 clinical trial at the ISDS conference. Capital, personnel and business relationships: not disclosed.

CounterpartyInternational Skeletal Dysplasia Society(ISDS)

An international organization established in Zurich, Switzerland, in 1999 to promote scientific advances in skeletal dysplasia and skeletal disorders. It holds an annual meeting every 2 years.

In this announcement the company addresses none of Contract Value / Offering price / Impact on Business Performance.

Source (materials cited by the company)

International Skeletal Dysplasia Society (ISDS) conference

Announced details
ItemDetails
Names of Products / Services Coveredumedaptanib pegol (anti-FGF2 aptamer)
CounterpartyInternational Skeletal Dysplasia Society(ISDS)
Counterparty overviewAn international organization established in Zurich, Switzerland, in 1999 to promote scientific advances in skeletal dysplasia and skeletal disorders. It holds an annual meeting every 2 years.
Relationship with the CompanyThe Company presented and discussed the results of its Phase 2 clinical trial at the ISDS conference. Capital, personnel and business relationships: not disclosed.
Applicable areaTreatment of achondroplasia (ACH)
Quantitative EffectsThe annual height-growth velocity of competing drugs is no more than +1.7 cm. If the Company's drug achieves an annual growth velocity of +2 to +3 cm or more in the Phase 3 trial, it could become a treatment option offering significant benefit.
SourceInternational Skeletal Dysplasia Society (ISDS) conference
Items this document does not state (11)
Contract ValueOffering priceContract DateLaunch dateAward/certification nameAwarding / certifying bodyRegistration number and expiry dateLocationLocation scaleUsage historyImpact on Business Performance

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.

To report to investors on the content presented and discussed at the ISDS conference. The company stated that umedaptanib pegol had achieved initial proof of concept and had attracted considerable interest from researchers and patients.

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Report on the International Skeletal Dysplasia Society Conference | RIBOMIC Inc. (4591) timely disclosure | Komori