Komori
Other Disclosures4591RIBOMIC Inc.Pharmaceuticals

An achondroplasia treatment (umedaptanib pegol): expansion of clinical trial sites in Japan (6 sites) in the domestic Phase III clinical trial

The number of trial sites approved by Institutional Review Boards for the domestic Phase III clinical trial of umedaptanib pegol has reached 6, making patient enrollment possible. The number of trial sites is expected to be expanded to a total of 16.

Worth reading
52Recurring
0–100. This measures how worthwhile something is to read, not how good or bad the company is.
Direction
Improvement
Direction inferred from the company’s description.
Scale
6
Sites (IRB-approved and open for patient enrollment)
Wording
Conditional
How definitive the wording is.

Announced details

umedaptanib pegol(RBM-007)
Applicable field (uses covered by this announcement)

Domestic Phase III clinical trial for pediatric patients with achondroplasia (ACH) aged 2–14

What the company reported numerically
Usage history

A cumulative total of 6 trial sites are now open for patient enrollment

Award/certification name

Orphan drug designation

Awarding / certifying body

Ministry of Health, Labour and Welfare

Location (as indicated in this announcement)

Locations of the trial sites shown on a map (individual locations are not provided in the text)

IRB approval obtained at a cumulative total of 6 medical institutions; expected to be expanded to a total of 16 sites
Impact on Business Performance

No impact on full-year earnings for the fiscal year ending March 2027

The company does not address Contract Value / Offering price.

Source (materials cited by the company)

The Company's disclosure dated 18 March 2026, "Notice of Clinical Trial Application for the Domestic Phase III Clinical Trial of the Achondroplasia Treatment (umedaptanib pegol)"

Announced details
ItemDetails
Names of Products / Services Coveredumedaptanib pegol(RBM-007)
Applicable areaDomestic Phase III clinical trial for pediatric patients with achondroplasia (ACH) aged 2–14
Award/certification nameOrphan drug designation
Awarding / certifying bodyMinistry of Health, Labour and Welfare
LocationLocations of the trial sites shown on a map (individual locations are not provided in the text)
Location scaleIRB approval obtained at a cumulative total of 6 medical institutions; expected to be expanded to a total of 16 sites
Usage historyA cumulative total of 6 trial sites are now open for patient enrollment
Impact on Business PerformanceNo impact on full-year earnings for the fiscal year ending March 2027
SourceThe Company's disclosure dated 18 March 2026, "Notice of Clinical Trial Application for the Domestic Phase III Clinical Trial of the Achondroplasia Treatment (umedaptanib pegol)"
Items this document does not state (9)
CounterpartyCounterparty overviewRelationship with the CompanyContract ValueOffering priceContract DateLaunch dateRegistration number and expiry dateQuantitative Effects

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.

Because achondroplasia is a rare disease with a limited patient population and the trial targets pediatric patients who are still growing, specialized expertise and careful management are required. The number of sites is expected to be expanded to a total of 16 to cover Japan nationwide.

How to read this page

This is not the documentKomori reads the disclosure the company filed and writes this summary. Figures are as stated by the company and are not audited.
Weight is not a verdictIt measures how much this changes what the company had already told the market. It is not a view on the shares.
Corrections happenIf the company reissues this disclosure, the page is rebuilt from the corrected version and the revision number moves up.
An achondroplasia treatment (umedaptanib pegol): expansion of clinical trial sites in Japan (6 sites) in the domestic Phase III clinical trial | RIBOMIC Inc. (4591) timely disclosure | Komori