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Other Disclosures4591RIBOMIC Inc.Pharmaceuticals

Notice Regarding Progress in Subject Enrollment in the Japanese Phase III Clinical Trial (WAKABA Trial) of the Treatment for Achondroplasia (umedaptanib pegol)

Enrollment of 2 additional subjects in the domestic Phase III clinical trial of umedaptanib pegol has been completed, bringing cumulative enrollment to 3 subjects. Preparations for conducting the trial have been completed at all 16 sites, and enrollment is progressing toward the target of 16 subjects.

Worth reading
44Recurring
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
3
Cumulative subject enrollment (subjects)
Wording
Definitive
How definitive the wording is.

Announced details

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

Treatment of pediatric patients with achondroplasia (ACH) aged 2 to 14 years; domestic Phase III clinical trial

What the company reported numerically
Usage history

Cumulative subject enrollment as of today: 3 subjects (enrollment of 2 additional subjects completed)

Award/certification name

Orphan drug designation

Awarding / certifying body

Ministry of Health, Labour and Welfare

Location (as indicated in this announcement)

All 16 sites (preparations for conducting the clinical trial completed)

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.

Announced details
ItemDetails
Names of Products / Services Coveredumedaptanib pegol(RBM-007)
Applicable areaTreatment of pediatric patients with achondroplasia (ACH) aged 2 to 14 years; domestic Phase III clinical trial
Award/certification nameOrphan drug designation
Awarding / certifying bodyMinistry of Health, Labour and Welfare
Location scaleAll 16 sites (preparations for conducting the clinical trial completed)
Usage historyCumulative subject enrollment as of today: 3 subjects (enrollment of 2 additional subjects completed)
Impact on Business PerformanceNo impact on full-year earnings for the fiscal year ending March 2027
Items this document does not state (11)
CounterpartyCounterparty overviewRelationship with the CompanyContract ValueOffering priceContract DateLaunch dateRegistration number and expiry dateLocationQuantitative EffectsSource

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.

Subject enrollment is being promoted in cooperation with each participating medical institution to achieve the target number of subjects.

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.
Notice Regarding Progress in Subject Enrollment in the Japanese Phase III Clinical Trial (WAKABA Trial) of the Treatment for Achondroplasia (umedaptanib pegol) | RIBOMIC Inc. (4591) timely disclosure | Komori