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Other Disclosures4588Oncolys BioPharma Inc.Pharmaceuticals

Notice of Publication of the LINE-1 Inhibitor Censavudine (OBP-601) in an International Medical Journal

Results from the phase IIa clinical trial of censavudine (OBP-601/TPN-101) in patients with PSP were published in the international medical journal Movement Disorders. The trial confirmed suppression of increases in NfL levels, as well as a decrease in NfL levels or no increase in the once-daily 400 mg group.

Worth reading
55In focus
0–100. This measures how worthwhile something is to read, not how good or bad the company is.
Direction
Neutral
Direction inferred from the company’s description.
Scale
42
Number of enrolled patients
Wording
Conditional
How definitive the wording is.

Announced details

Censavudine (OBP-601/TPN-101)
Applicable field (uses covered by this announcement)

Neurodegenerative diseases, including progressive supranuclear palsy (PSP)

What the company reported numerically
Quantitative Effects

Suppression of increases in NfL levels in cerebrospinal fluid. In the group switched from placebo to once-daily 400 mg dosing, NfL levels decreased from Week 24. In the group that continued once-daily 400 mg dosing for 48 weeks from baseline, NfL levels did not increase.

Usage history

42 patients with PSP enrolled in the trial

Relationship between the counterparty and the company
Oncolys BioPharma Inc.4588
Relationship with the Company

The counterparty to which our company out-licensed OBP-601. The company is developing it for neurodegenerative diseases.

CounterpartyTransposon Therapeutics, Inc
Impact on Business Performance

There will be no impact on the financial results for the fiscal year ending December 2026.

The company does not address Contract Value / Offering price.

Source (materials cited by the company)

International medical journal Movement Disorders, August 2026 issue

Announced details
ItemDetails
Names of Products / Services CoveredCensavudine (OBP-601/TPN-101)
CounterpartyTransposon Therapeutics, Inc
Relationship with the CompanyThe counterparty to which our company out-licensed OBP-601. The company is developing it for neurodegenerative diseases.
Applicable areaNeurodegenerative diseases, including progressive supranuclear palsy (PSP)
Quantitative EffectsSuppression of increases in NfL levels in cerebrospinal fluid. In the group switched from placebo to once-daily 400 mg dosing, NfL levels decreased from Week 24. In the group that continued once-daily 400 mg dosing for 48 weeks from baseline, NfL levels did not increase.
Usage history42 patients with PSP enrolled in the trial
Impact on Business PerformanceThere will be no impact on the financial results for the fiscal year ending December 2026.
SourceInternational medical journal Movement Disorders, August 2026 issue
Items this document does not state (10)
Counterparty overviewContract ValueOffering priceContract DateLaunch dateAward/certification nameAwarding / certifying bodyRegistration number and expiry dateLocationLocation scale

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.

The results of the phase IIa clinical trial were published in the August 2026 issue of the international medical journal Movement Disorders.

How to read this page

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Notice of Publication of the LINE-1 Inhibitor Censavudine (OBP-601) in an International Medical Journal | Oncolys BioPharma Inc. (4588) timely disclosure | Komori