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Other Disclosures4588Oncolys BioPharma Inc.Pharmaceuticals

Notice of the 24-month stability test results for the oncolytic virus Telomelysin Injection

All quality test items for Telomelysin® Injection met the required standards in the 24-month stability study. Accordingly, the second commercial batch, scheduled for shipment in 2027, is expected to be supplied with a 24-month shelf life.

Worth reading
48Recurring
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
24
months (shelf life and stability study period)
Wording
Conditional
How definitive the wording is.

Announced details

Telomelysin® Injection (generic name: suratadenoturev; development code: OBP-301)
Applicable field (uses covered by this announcement)

Treatment of esophageal cancer

Launch dateSales have begun. Start date: Not disclosed
What the company reported numerically
Quantitative Effects

All quality test items met the required standards in the 24-month stability study. The company stated that this will increase flexibility in inventory management and make a significant contribution to stable supply to medical institutions.

Registration number and expiry date

24-month shelf life (second commercial batch scheduled for shipment in 2027)

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

Announced details
ItemDetails
Names of Products / Services CoveredTelomelysin® Injection (generic name: suratadenoturev; development code: OBP-301)
Launch dateSales have begun. Start date: Not disclosed
Applicable areaTreatment of esophageal cancer
Registration number and expiry date24-month shelf life (second commercial batch scheduled for shipment in 2027)
Quantitative EffectsAll quality test items met the required standards in the 24-month stability study. The company stated that this will increase flexibility in inventory management and make a significant contribution to stable supply to medical institutions.
Items this document does not state (13)
CounterpartyCounterparty overviewRelationship with the CompanyContract ValueOffering priceContract DateAward/certification nameAwarding / certifying bodyLocationLocation scaleUsage historyImpact on Business PerformanceSource

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.

All quality test items met the required standards in the 24-month stability study. The company stated that this will increase flexibility in inventory management and contribute to stable supply to medical institutions.

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 of the 24-month stability test results for the oncolytic virus Telomelysin Injection | Oncolys BioPharma Inc. (4588) timely disclosure | Komori