Recent blog posts
Market Analysis of Aceclofenac in the USA: Opportunities and Barriers for Market Entry
Drug Insights
6 min read
Market Analysis of Aceclofenac in the USA: Opportunities and Barriers for Market Entry
29 August 2025
Aceclofenac is a widely used NSAID in Europe and China but remains unapproved in the USA. Explore its global approvals, patent landscape, clinical results, and strategies for US market entry.
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Market Analysis of Succinylcholine Chloride in the USA: Opportunities and Patent Landscape
Drug Insights
6 min read
Market Analysis of Succinylcholine Chloride in the USA: Opportunities and Patent Landscape
29 August 2025
Succinylcholine Chloride has been in the US market since 1952 as a key anesthetic agent. Explore its approvals, clinical results, patent barriers, and strategies for market entry and innovation.
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Market Analysis of Sofosbuvir (Sovaldi) in the USA: Patents, Exclusivity, and Entry Opportunities
Drug Insights
6 min read
Market Analysis of Sofosbuvir (Sovaldi) in the USA: Patents, Exclusivity, and Entry Opportunities
28 August 2025
Comprehensive market analysis of Sofosbuvir (Sovaldi) in the USA, covering FDA approvals, patents, exclusivity, clinical insights, and strategic recommendations for market entry.
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Inclisiran Market Analysis in the USA: Patents, Exclusivity, and Market Entry Outlook
Drug Insights
6 min read
Inclisiran Market Analysis in the USA: Patents, Exclusivity, and Market Entry Outlook
28 August 2025
Comprehensive analysis of Inclisiran in the USA, covering FDA approvals, patents, clinical results, regulatory exclusivity, and strategic insights for innovators and potential generic challengers.
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Dobutamine Hydrochloride Market Analysis in the USA: Generic Landscape, Patents, and Clinical Insights
Drug Insights
6 min read
Dobutamine Hydrochloride Market Analysis in the USA: Generic Landscape, Patents, and Clinical Insights
27 August 2025
Comprehensive market analysis of Dobutamine Hydrochloride in the USA, including FDA approvals, patent barriers, clinical data, regulatory risks, and strategic recommendations for generic manufacturers.
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Lacosamide Market Analysis in the USA: Patent Landscape, Clinical Insights, and Strategic Entry
Drug Insights
6 min read
Lacosamide Market Analysis in the USA: Patent Landscape, Clinical Insights, and Strategic Entry
27 August 2025
Explore the US market analysis of Lacosamide, including FDA approvals, patent landscape, clinical results, regulatory risks, and strategic recommendations for generic and innovator companies.
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Amisulpride Market Landscape: Patent Barriers, Clinical Insights, and Global Entry Strategies
Drug Insights
6 min read
Amisulpride Market Landscape: Patent Barriers, Clinical Insights, and Global Entry Strategies
26 August 2025
Discover the global market landscape of Amisulpride, including patent barriers, clinical insights, regulatory risks, and strategic opportunities in the US, China, and EU markets.
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Overview of Fixed-Dose Combination Drug Approvals in South Korea – March 2025
Drug Insights
17 min read
Overview of Fixed-Dose Combination Drug Approvals in South Korea – March 2025
24 April 2025
In March 2025, South Korea’s Ministry of Food and Drug Safety (MFDS) approved a total of 6 new FDCs across multiple therapeutic areas.
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Suzetrigine: FDA-Approved Nav1.8 Inhibitor Offers Breakthrough Non-Opioid Relief for Moderate to Severe Acute Pain
Drug Insights
3 min read
Suzetrigine: FDA-Approved Nav1.8 Inhibitor Offers Breakthrough Non-Opioid Relief for Moderate to Severe Acute Pain
14 February 2025
Suzetrigine received approval from the FDA on January 30, 2025, as a small-molecule pharmaceutical for the treatment of moderate to severe acute pain in adults.
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FDA-Approved Combination of Meloxicam and Rizatriptan Offers Dual-Action Relief for Migraine Treatment
Drug Insights
4 min read
FDA-Approved Combination of Meloxicam and Rizatriptan Offers Dual-Action Relief for Migraine Treatment
14 February 2025
The combination drug Meloxicam and Rizatriptan, received approval from the U.S. Food and Drug Administration (FDA) on January 30, 2025, for the treatment of migraine.
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Limertinib: A Novel Third-Generation EGFR-TKI Approved in China
Drug Insights
3 min read
Limertinib: A Novel Third-Generation EGFR-TKI Approved in China
14 February 2025
Limertinib is a newly developed small-molecule chemical drug, specifically designed as an inhibitor targeting the epidermal growth factor receptor (EGFR) T790M mutation.
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Senaparib: A Next-Generation PARP1/2 Inhibitor Approved in China
Drug Insights
3 min read
Senaparib: A Next-Generation PARP1/2 Inhibitor Approved in China
14 February 2025
Senaparib is a next-generation, highly potent PARP1/2 inhibitor developed by IMPACT Therapeutics.
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