With the launch of an adalimumab, Cadila hopes to get a piece of the worldwide biosimilar market for antirheumatic treatments.
Continuing with its string of recent biosimilar launches, Cadila Pharmaceuticals has put an adalimumab biosimilar (Cadalimab) on the Indian market. The drug is available in a prefilled syringe, 40 mg/0.8 ml.
Adalimumab is an antirheumatic drug for the treatment of arthritis, plaque psoriasis, ankylosing spondylitis, Crohn disease, and ulcerative colitis. It references Humira, an AbbVie product, which had net revenues in 2019 of $19.2 billion, $14.9 billion of that in the United States, where the product does not yet face biosimilar competition. By binding with tumor necrosis factor-alpha, the drug helps to prevent inflammation.
A Large Potential Market
There is a potentially large market for Cadalimab. Cadila, based in Ahmedabad, India, noted that roughly 7 million individuals in India have rheumatoid arthritis (RA) and 2.8% of the population has psoriasis. Adalimumab is currently marketed in over 60 countries by multiple companies, according to Transparency Market Research, which noted that the high cost of adalimumab ($2000-$3000 per month) is a barrier to uptake.
In the United States, 6 adalimumab biosimilars have been approved but market entry is not anticipated for any of them before 2023, owing to product exclusivity rights. Mordor Intelligence has forecast an anual growth rate for the adalimumab of 5.1% through 2025, predicting the fastest growth for adalimumab biosimilars in the Asia Pacific region, including India and China, where health care consumers are highly responsive to price changes.
“While these are not life-threatening, psoriasis and RA can be painful to live with. With the launch of Cadalimab, we want to reach these patients with a cost-effective solution and give them a chance at a better life,” Amit Ajmera, company vice president, said in a statement.
Cadila noted this marks the fourth biosimilar launch in the past 2 months. In early August 2020, Cadila launched a teriparatide biosimilar (NuPTH), referencing Lilly’s Forteo, for the treatment of osteoporosis.
In late July, Cadila launched a rituximab (Ritucad), for the treatment of blood cancer, including non-Hodgkin lymphoma, and rheumatoid arthritis, and a bevacizumab (Bevaro), for the treatment of ovarian cancer, glioblastoma multiforme, colorectal cancer, breast cancer, lung cancer, cervical cancer, and kidney cancer. The rituximab biosimilar references Rituxan (Biogen) and the bevacizumab biosimilar, Avastin (Genentech).
Cadila, one of the largest privately held pharmaceutical companies in India, suggested it may have more biosimilar products to launch later this year.
Biosimilars in America: Overcoming Barriers and Maximizing Impact
July 21st 2024Join us as we explore the complexities of the US biosimilars market, discussing legislative influences, payer and provider adoption factors, and strategies to overcome industry challenges with expert insights from Kyle Noonan, PharmD, MS, value & access strategy manager at Cencora.
Patient-Reported Outcomes Similar Between Adalimumab-adbm, Reference Product in VOLTAIRE-RA Study
September 28th 2024A summary of research written by Vibeke Strand, MD, clinical professor in division of immunology/rheumatology at Stanford University School of Medicine, gave an overview of patient-reported outcomes (PROs) in the VOLTAIRE-RA trial.
Biosimilars Oncology Roundup for June 2024—Podcast Edition
July 7th 2024On this episode of Not So Different, we review biosimilar news coming out of June, with clinical trial results from conferences and a study showcasing how to overcome economic and noneconomic barriers to oncology biosimilars.
AAM Report: Despite Massive Savings, Patient OOP Costs on Biosimilars, Generics Remain High, Part 2
September 24th 2024Part 2 of our series diving into the Association for Accessible Medicines' (AAM) latest report discusses that while generics and biosimilars saved $445 billion in 2023, their potential is hindered by high patient costs, drug shortages, and ineffective policies, underscoring the need for reforms to fully realize their benefits.