Keymed Biosciences Announces Strong 2025 Interim Results

Keymed Biosciences Reports Impressive Interim Results for 2025

Keymed Biosciences Inc. (02162.HK) has showcased outstanding interim results for the year, reflecting strong momentum in both commercialization and research and development. The company’s performance has raised expectations for its future endeavors in the biopharmaceutical sector.

Record Revenue Driven by Core Products

This reporting period marked a significant financial achievement for Keymed, with revenues hitting record highs, tied closely to the success of its flagship product, Stapokibart, an innovative IL-4R? antibody. Marketed as Kang Yue Da, this product generated net sales of approximately RMB 170 million, indicating a robust demand in the market.

Strategic Financing and Pipeline Development

Strengthening its financial position, Keymed successfully secured a substantial placement, raising approximately HK$864 million. This influx of capital positions the company to enhance its pipeline development and commercialization strategies effectively. The successful financing endeavors ensure that Keymed can sustain its momentum in research and development.

Advancements in the R&D Pipeline

The company's differentiated research and development pipeline has made substantial progress, with several key highlights: Stapokibart is currently expanding its indications beyond adult atopic dermatitis and includes ongoing Phase III trials targeting pediatric atopic dermatitis and prurigo nodularis.

Partnership and Licenses for Future Growth

In an exciting partnership, AstraZeneca was granted an exclusive global license for CMG901 (AZD0901), a Claudin 18.2 antibody-drug conjugate. AstraZeneca is currently advancing in global Phase II/III trials for various cancer types, including gastric, pancreatic, and biliary tract cancers. This collaborative approach enhances Keymed’s research capabilities and pathway into markets internationally.

Innovative Antibody Development

Additionally, Keymed is advancing with CM512, a TSLP x IL-13 bispecific antibody, which is currently in Phase II trials for atopic dermatitis and chronic rhinosinusitis with nasal polyps. With a focus on patient-centric solutions, these developments are expected to fulfill significant unmet medical needs.

Recognition in Academic Circles

Keymed's impact extends beyond commercial achievements to significant academic contributions. The company’s research has been highlighted in prestigious scientific journals, including The New England Journal of Medicine, Nature Medicine, and JAMA for critical studies regarding Stapokibart. Furthermore, this product has been incorporated into treatment guidelines in national healthcare protocols.

Positioned for Future Success

With strong cash reserves, strategic financing, and a well-defined clinical pipeline, Keymed Biosciences is not only competitive but is also delivering high-quality, affordable therapies. The commitment to innovation ensures that patients in China and around the globe have access to transformative solutions in healthcare.

Frequently Asked Questions

What were the major highlights from Keymed's interim report for 2025?

Keymed reported record revenues driven by its core product, Stapokibart, with substantial advancements in its R&D pipeline.

How much revenue did Keymed generate during this period?

The company generated approximately RMB 170 million in net sales.

What strategic actions did Keymed take to strengthen its finances?

Keymed successfully raised about HK$864 million through placements to boost its development funds.

What products are Keymed currently developing?

Keymed is expanding Stapokibart's indications and progressing CMG901 and CM512 through clinical trials.

In which academic publications has Keymed's research been featured?

Research from Keymed has been published in high-impact journals such as The New England Journal of Medicine and Nature Medicine.

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