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Other Disclosures4588Oncolys BioPharma Inc.Pharmaceuticals

Notice regarding the submission of a clinical trial notification for a new indication of the oncolytic virus Telomelysin (laryngeal and pharyngeal cancer)

A clinical trial notification was submitted to the PMDA for a Phase 2 clinical trial of Telomelysin (OBP-301) in combination with radiotherapy for laryngeal and pharyngeal cancer. Administration is planned to begin in the first half of 2027.

Worth reading
65In focus
Scored from 5 of 6 sections
Direction
Neutral
Direction inferred from the company’s description.
Scale
—
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Wording
Conditional
How definitive the wording is.

Announced details

Oncolytic virus Telomelysin (development code: OBP-301)
Applicable field (uses covered by this announcement)

Laryngeal and pharyngeal cancer. Administration in combination with radiotherapy.

Launch dateAdministration scheduled to begin in the first half of 2027
Relationship between the counterparty and the company
Oncolys BioPharma Inc.4588
Relationship with the Company

The PMDA is the recipient of the clinical trial notification. A clinical trial network has been established with research groups at Kyoto Prefectural University of Medicine and others. Capital and personnel relationships have not been disclosed.

CounterpartyPharmaceuticals and Medical Devices Agency (PMDA), research groups at Kyoto Prefectural University of Medicine, and others

The PMDA is the Pharmaceuticals and Medical Devices Agency. No information beyond the summary stated in the filing has been disclosed regarding the research groups at Kyoto Prefectural University of Medicine and others.

Impact on Business Performance

The impact on results for the fiscal year ending December 2026 is minor

The company does not address Contract Value / Offering price.

Announced details
ItemDetails
Names of Products / Services CoveredOncolytic virus Telomelysin (development code: OBP-301)
CounterpartyPharmaceuticals and Medical Devices Agency (PMDA), research groups at Kyoto Prefectural University of Medicine, and others
Counterparty overviewThe PMDA is the Pharmaceuticals and Medical Devices Agency. No information beyond the summary stated in the filing has been disclosed regarding the research groups at Kyoto Prefectural University of Medicine and others.
Relationship with the CompanyThe PMDA is the recipient of the clinical trial notification. A clinical trial network has been established with research groups at Kyoto Prefectural University of Medicine and others. Capital and personnel relationships have not been disclosed.
Launch dateAdministration scheduled to begin in the first half of 2027
Applicable areaLaryngeal and pharyngeal cancer. Administration in combination with radiotherapy.
Impact on Business PerformanceThe impact on results for the fiscal year ending December 2026 is minor
Items this document does not state (11)
Contract ValueOffering priceContract DateAward/certification nameAwarding / certifying bodyRegistration number and expiry dateLocationLocation scaleQuantitative EffectsUsage historySource

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 develop Telomelysin for laryngeal and pharyngeal cancer with the aim of preserving the vocal cords.

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 the submission of a clinical trial notification for a new indication of the oncolytic virus Telomelysin (laryngeal and pharyngeal cancer) | Oncolys BioPharma Inc. (4588) timely disclosure | Komori