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Thursday, June 11, 2026

Tag: 7

Aduro Clean Technologies Announces Pricing of US$15.64 Million Underwritten Public Offering and Concurrent Private Placement of up to US$7.17 Million

Aduro announces pricing of up to US$22.81M offering, including a public offering and LIFE private placement to fund FOAK Plant, R&D and corporate purposes.

Free Camping: The Dyrt Finds 3 Out of 5 Campers Camp for Free

PORTLAND, Ore., June 10, 2026 /PRNewswire/ -- The Dyrt, the app to get the best campsites, built by the largest RVing and camping community...

InMotion Hosting Enhances Global Network with High-Speed Established Peering Partnerships

SDN fabric integration across the company's Los Angeles, Ashburn, and Amsterdam peering points turns three regional interconnection hubs into on-demand gateways to the global...

Immunic to Participate in Investor, Industry and Scientific Conferences in June

NEW YORK, June 10, 2026 /PRNewswire/ -- Immunic, Inc. (Nasdaq: IMUX), a late-stage biotechnology company pioneering the development of novel oral therapies for neurologic diseases,...

Italfarmaco Announces Health Canada Acceptance and Priority Review of New Drug Submission for Givinostat as a Duchenne Muscular Dystrophy Treatment

MILAN, Italy, June 10, 2026Italfarmaco S.p.A. today announced that Health Canada has accepted for review the New Drug Submission (NDS) for givinostat (Duvyzat®) for the treatment of Duchenne muscular dystrophy (DMD). Health Canada has granted givinostat Priority Review status, a designation reserved for drugs that may provide a significant improvement in the benefit-risk profile over existing therapies.

“Families affected by Duchenne muscular dystrophy in Canada currently have limited access to treatment options that can slow functional decline,” said Dr. Jean K. Mah, a Canadian investigator for the EPIDYS and OLE studies and Director of the Pediatric Neuromuscular Program at the Alberta Children’s Hospital in Calgary, Alberta. “As a clinician treating DMD patients, I am encouraged by this positive step in the Canadian regulatory progress and givinostat’s therapeutic potential demonstrated in the EPIDYS Phase 3 study."

An estimated 1000 boys in Canada are living with DMD, one of the most severe and common forms of childhood muscular dystrophy.1 As part of its commitment to the Canadian DMD community, Italfarmaco will establish a local Canadian affiliate to lead ongoing discussions with health authorities throughout the regulatory review process and to support patients and their families as well as healthcare providers. Subject to Health Canada’s review, marketing authorisation could be granted before the end of 2026.

“Duchenne muscular dystrophy places an enormous burden on boys and their families, and we understand the urgency of bringing new treatment options to communities where significant unmet need remains,” said Francesco Di Marco, Chief Executive Officer of Italfarmaco Group. “Health Canada’s acceptance of the New Drug Submission for givinostat with Priority Review is an encouraging step forward. As we expand our presence in Canada, we are committed to working with clinicians, patient organisations, and other stakeholders to support the Duchenne community and help advance access for appropriate patients, if approved.”

The submission builds on many years of clinical research, including contributions from Canadian patients, families, investigators, and three clinical trial sites in Canada. It is supported by data from the EPIDYS Phase 3 multicentre, randomized, double-blind, placebo-controlled trial (NCT02851797) evaluating givinostat in ambulant boys with DMD aged six and older. The study met its primary endpoint, demonstrating a statistically significant and clinically meaningful difference in time to complete the four-stair climb assessment in patients treated with givinostat twice daily, in addition to corticosteroids, compared to placebo and corticosteroids. During the study, the most common treatment-related adverse events (frequency ≥1/10 boys) associated with givinostat were decreased platelet count/thrombocytopenia, increased blood triglyceride/hypertriglyceridemia, diarrhoea and abdominal pain; none of the severe or serious adverse events were treatment-related or resulted in study withdrawal. givinostat tolerability was managed with appropriate monitoring and dose adjustments. No other safety concerns were observed.2 Patients from the EPIDYS study remain under observation in a long-term study assessing tolerability and efficacy, with follow-up extending up to eleven years (NCT03373968).

Givinostat has received regulatory approvals in multiple regions, including the US, the UK, the EU, and the UAE for the treatment of DMD. Additional regulatory submissions are ongoing in other geographies, reflecting Italfarmaco’s commitment to enabling access for as many individuals living with DMD as possible.


About Duchenne Muscular Dystrophy

New Case Series on Umbilical Tissue in Plantar Fascia Applications Demonstrates Clinical Reproducibility

Case Series by Dr. Robert Parker, DPM, Published in Archives of Clinical...

Tokenized Cash Management Advisory Group Publishes the Scope of Its Work Program

The practitioner-led group sets out the use cases, participants, and capabilities required to take tokenized cash management from pilots into production.LONDON and NEW YORK,...

Transaction in Own Shares

Transaction in Own Shares

Telenor acquires Enivest in Western Norway

Telenor has agreed to acquire Enivest, one of the leading fibre operators in Western Norway, in a transaction valued at NOK 2.5 billion

Japanese Contemporary Artist Takuma Tanaka Unveils “Don’t Think, Feel” Solo Exhibition at The Wall Art Gallery in Miami’s Wynwood

New body of vibrant, expressive paintings explores consciousness, intuition, and the power of feeling — featuring powerful works incorporating Bruce Lee's iconic philosophy; artist...

JETOUR’s Return of the Cheetah: Horn of Africa Wins Telly Awards

WUHU, China, June 09, 2026 (GLOBE NEWSWIRE) -- The winners of the 47th Telly Awards were officially announced. Return of the Cheetah: Horn of Africa, a public welfare documentary co-produced by JETOUR and DISCOVERY Channel, received three major honors, including Gold Winner in General-Documentary: Short Form, Silver Winner in Craft-Videography & Cinematography, and Silver Winner in General-Nature & Wildlife. The film also won a Gold Tower Award at the New York Festivals Advertising Awards, earning international recognition for its outstanding production quality and commitment to wildlife conservation.

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