Tardive Dyskinesia Treatment Market Updates

Skyquest Technology's expert advisors continuously track and analyze the latest developments and updates related to tardive dyskinesia treatment market. Our team of analysts stay abreast of all the recent news stories shaping the industry including new product launches by major companies, strategic partnerships, M&As, Patent filings and industry and regulatory developments.

Tardive Dyskinesia Treatment Market News

in Tardive Dyskinesia Treatment Market
  • In November 2024, Teva Pharmaceuticals, a leading pharmaceutical company announced new patient- and physician-reported interim results from the Phase 4 IMPACT-TD Registry study. The study evaluated holistic effects of TD, showing real-world treatment patterns and outcomes with once-daily AUSTEDO® XR® (deutetrabenazine) extended-release tablets.
  • In May 2024, the United States Food and Drug Administration (FDA) announced that it had approved Teva Pharmaceuticals’ Austedo XR (deutetrabenazine) as a once-daily pill treatment option for indicated in adults for tardive dyskinesia (TD) and Huntington disease (HD) chorea control.

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Global Tardive Dyskinesia Treatment Market size was valued at USD 9.75 Billion in 2023 and is poised to grow from USD 10.11 Billion in 2024 to USD 13.52 Billion by 2032, growing at a CAGR of 3.7% during the forecast period (2025-2032).

Tardive dyskinesia treatment providers should focus on investing in R&D to develop new therapeutics and treatments. Working with government organizations and health non-profits can also expand the business scope for market players. Developing treatment with minimal side effects is a key opportunity as per the global tardive dyskinesia treatment market analysis. 'Teva Pharmaceutical Industries Ltd.', 'Neurocrine Biosciences Inc.', 'Medicure Inc.', 'Mylan N.V', 'Dr. Reddy’s Laboratories Ltd.', 'Sun Pharmaceutical Industries Ltd. ', 'Bionpharma', 'Hetero', 'Bausch Health', 'Sanofi', 'Johnson & Johnson Services Inc.', 'GlaxoSmithKline Plc.', 'Lupin Pharmaceuticals Inc.', 'Lilly', 'Novartis AG'

Regulatory agencies, notably the U.S. Food and Drug Administration (FDA), have adopted expedited pathways for TD treatments, recognizing the unmet medical need. Fast-track designations and priority reviews facilitate quicker market entry for promising therapies. This regulatory support incentivizes pharmaceutical companies to invest in TD drug development and favors the global tardive dyskinesia treatment market outlook as well.

Advancements in VMAT2 Inhibitor Therapies: The development and approval of vesicular monoamine transporter 2 (VMAT2) inhibitors, such as valbenazine (Ingrezza) and deutetrabenazine (Austedo), have revolutionized TD treatment. These medications specifically target the underlying mechanisms of TD, offering improved efficacy and safety profiles compared to traditional therapies. The introduction of alternative formulations, like Ingrezza Sprinkle, caters to patients with swallowing difficulties, enhancing treatment adherence. Hence, focusing on advancement of therapies is slated to be a top tardive dyskinesia treatment market trend in the long run.

Why is the Adoption Rate of Tardive Dyskinesia Treatment High in North America?

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Global Tardive Dyskinesia Treatment Market
Tardive Dyskinesia Treatment Market

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