Komori
Occurring Fact4582SymBio Pharmaceuticals LimitedPharmaceuticals

Summary of Financial Results for the First Quarter of the Fiscal Year Ending December 2026 [Japanese GAAP] (Consolidated)

In the first quarter of the fiscal year ending December 2026, sales of TREAKISYN declined due to a drug price revision and the growing penetration of generic products. Combined with higher research and development expenses, this resulted in an operating loss of ¥2,341 million and a quarterly net loss attributable to owners of the parent of ¥2,401 million, with losses widening from the same period of the previous year. While significant uncertainty remains regarding the going concern assumption, the full-year earnings forecast remains unchanged.

Worth reading
59In focus
Scored from 4 of 5 sections
Direction
Deterioration
Direction inferred from the company’s description.
Scale
2401.405
Millions of yen (quarterly net loss attributable to owners of the parent)
Wording
Avoiding a definitive answer
How definitive the wording is.

Consolidated results for the first quarter of the fiscal year ending December 2026

Subject Entity

SymBio Pharmaceuticals Limited and its group companies

Target Locations / Products

TREAKISYN® IV infusion 100 mg/4 mL [RTD (Ready-To-Dilute) formulation], BCV (brincidofovir), and the IVD business

Occurrence31 March 2026 (end of the first-quarter consolidated accounting period)
This disclosure05/07/2026
Cause

Revenue from TREAKISYN declined due to the impact of a drug price revision and the growing penetration of generic products. Research and development expenses also increased as research and development activities for the global Phase III clinical trial targeting adenovirus infection after hematopoietic stem cell transplantation entered full-scale operation.

Amount of Impact on Business Performance

Revenue: ¥233,463 thousand; operating loss: ¥2,341,115 thousand; ordinary loss: ¥2,390,608 thousand; quarterly net loss attributable to owners of the parent: ¥2,401,405 thousand (first quarter of the fiscal year ending December 2026)

Accounting period in which recognized

First quarter of the fiscal year ending December 2026 (1 January 2026–31 March 2026)

Impact on Earnings Forecast

The consolidated earnings forecast for the fiscal year ending December 2026 is unchanged from the forecast announced on 5 February 2026. The full-year forecast is revenue of ¥3,891 million, an operating loss of ¥4,231 million, an ordinary loss of ¥4,291 million, and a net loss attributable to owners of the parent of ¥4,331 million.

Company response

Suspended operations

The international joint Phase Ib clinical trial targeting patients with malignant lymphoma is currently on temporary hold.

Outlook

The company will continue clinical development of BCV, research and development for multiple indications, early commercialization of the IVD business, securing funding through equity financing and other means, collaboration and business alliances with other companies, cost management and expense reductions, and optimization of its fixed-cost structure. However, uncertainty remains regarding the progress of research and development, the success of partnering and business alliances, and the funding environment.

Event that occurred
ItemDetails
Event nameConsolidated results for the first quarter of the fiscal year ending December 2026
Date of occurrence31 March 2026 (end of the first-quarter consolidated accounting period)
Subject EntitySymBio Pharmaceuticals Limited and its group companies
Target Locations / ProductsTREAKISYN® IV infusion 100 mg/4 mL [RTD (Ready-To-Dilute) formulation], BCV (brincidofovir), and the IVD business
CauseRevenue from TREAKISYN declined due to the impact of a drug price revision and the growing penetration of generic products. Research and development expenses also increased as research and development activities for the global Phase III clinical trial targeting adenovirus infection after hematopoietic stem cell transplantation entered full-scale operation.
Amount of Impact on Business PerformanceRevenue: ¥233,463 thousand; operating loss: ¥2,341,115 thousand; ordinary loss: ¥2,390,608 thousand; quarterly net loss attributable to owners of the parent: ¥2,401,405 thousand (first quarter of the fiscal year ending December 2026)
Accounting period in which recognizedFirst quarter of the fiscal year ending December 2026 (1 January 2026–31 March 2026)
Impact on Earnings ForecastThe consolidated earnings forecast for the fiscal year ending December 2026 is unchanged from the forecast announced on 5 February 2026. The full-year forecast is revenue of ¥3,891 million, an operating loss of ¥4,231 million, an ordinary loss of ¥4,291 million, and a net loss attributable to owners of the parent of ¥4,331 million.
Suspended operationsThe international joint Phase Ib clinical trial targeting patients with malignant lymphoma is currently on temporary hold.
OutlookThe company will continue clinical development of BCV, research and development for multiple indications, early commercialization of the IVD business, securing funding through equity financing and other means, collaboration and business alliances with other companies, cost management and expense reductions, and optimization of its fixed-cost structure. However, uncertainty remains regarding the progress of research and development, the success of partnering and business alliances, and the funding environment.
Items this document does not state (15)
Date recognized / date notice receivedType of litigation or proceedingCourt or authorityPlaintiffDefendantDate of filing / date of actionClaim amount / surcharge amountAmount of receivables at risk of non-collection or delayed collectionScheduled resumption dateInvestigation structureMeasures to prevent recurrenceDirectors' and officers' liabilityVoting rights ownership percentage before the changeVoting rights ownership percentage after the changePlanned follow-up disclosure

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.

Revenue from TREAKISYN declined due to the impact of a drug price revision and the growing penetration of generic products. Research and development activities for the global Phase III clinical trial targeting adenovirus infection after hematopoietic stem cell transplantation entered full-scale operation, resulting in higher research and development expenses. The company also explains that its research and development-driven business requires substantial research and development expenses and considerable time before products can be commercialized and generate revenue.

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.
Summary of Financial Results for the First Quarter of the Fiscal Year Ending December 2026 [Japanese GAAP] (Consolidated) | SymBio Pharmaceuticals Limited (4582) timely disclosure | Komori