Recent blog posts
Dorzagliatin Drug Asset Due Diligence Report 2026: Clinical, IP, Market, Deals, and Go/No-Go
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8 min read
Dorzagliatin Drug Asset Due Diligence Report 2026: Clinical, IP, Market, Deals, and Go/No-Go
21 July 2026
Dorzagliatin: Approved. 2026 diligence verdict: GO. Evidence review covers clinical, IP, deals, and risks.
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Lansoprazole/Sodium Bicarbonate Drug Asset Due Diligence Report 2026: Clinical, IP, Market, Deals, and Go/No-Go
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8 min read
Lansoprazole/Sodium Bicarbonate Drug Asset Due Diligence Report 2026: Clinical, IP, Market, Deals, and Go/No-Go
21 July 2026
Lansoprazole/Sodium Bicarbonate: Approved. 2026 diligence verdict: GO. Evidence review covers clinical, IP, deals, and risks.
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Serplulimab Biologics Sequence Review Report 2026: PD-1 Similarity and Patent-Risk Signals
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6 min read
Serplulimab Biologics Sequence Review Report 2026: PD-1 Similarity and Patent-Risk Signals
21 July 2026
Sequence similarity, pairwise alignment, patent-sequence and antibody–antigen evidence for Serplulimab, a antibody targeting PD-1.
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Toludesvenlafaxine Hydrochlorid Drug Asset Due Diligence Report 2026: Clinical, IP, Market, Deals, and Go/No-Go
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8 min read
Toludesvenlafaxine Hydrochlorid Drug Asset Due Diligence Report 2026: Clinical, IP, Market, Deals, and Go/No-Go
21 July 2026
Toludesvenlafaxine Hydrochlorid: Approved. 2026 diligence verdict: GO. Evidence review covers clinical, IP, deals, and risks.
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Elasomeran/Davesomeran Drug Asset Due Diligence Report 2026: Clinical, IP, Market, Deals, and Go/No-Go
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8 min read
Elasomeran/Davesomeran Drug Asset Due Diligence Report 2026: Clinical, IP, Market, Deals, and Go/No-Go
21 July 2026
Elasomeran/Davesomeran: Approved. 2026 diligence verdict: GO. Evidence review covers clinical, IP, deals, and risks.
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Linperlisib Drug Asset Due Diligence Report 2026: Clinical, IP, Market, Deals, and Go/No-Go
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8 min read
Linperlisib Drug Asset Due Diligence Report 2026: Clinical, IP, Market, Deals, and Go/No-Go
21 July 2026
Linperlisib: Approved. 2026 diligence verdict: GO. Evidence review covers clinical, IP, deals, and risks.
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Immune globulin intravenous, Human-dira Drug Asset Due Diligence Report 2026: Clinical, IP, Market, Deals, and Go/No-Go
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8 min read
Immune globulin intravenous, Human-dira Drug Asset Due Diligence Report 2026: Clinical, IP, Market, Deals, and Go/No-Go
21 July 2026
Immune globulin intravenous, Human-dira: Approved. 2026 diligence verdict: GO. Evidence review covers clinical, IP, deals, and risks.
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Retifanlimab Biologics Sequence Review Report 2026: PD-1 Similarity and Patent-Risk Signals
Latest Hotspot
6 min read
Retifanlimab Biologics Sequence Review Report 2026: PD-1 Similarity and Patent-Risk Signals
21 July 2026
Sequence similarity, pairwise alignment, patent-sequence and antibody–antigen evidence for Retifanlimab, a antibody targeting PD-1.
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Para-Toluenesulfonamide Drug Asset Due Diligence Report 2026: Clinical, IP, Market, Deals, and Go/No-Go
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8 min read
Para-Toluenesulfonamide Drug Asset Due Diligence Report 2026: Clinical, IP, Market, Deals, and Go/No-Go
21 July 2026
Para-Toluenesulfonamide: Approved. 2026 diligence verdict: GO. Evidence review covers clinical, IP, deals, and risks.
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Enavogliflozin Drug Asset Due Diligence Report 2026: Clinical, IP, Market, Deals, and Go/No-Go
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8 min read
Enavogliflozin Drug Asset Due Diligence Report 2026: Clinical, IP, Market, Deals, and Go/No-Go
21 July 2026
Enavogliflozin: Approved. 2026 diligence verdict: GO. Evidence review covers clinical, IP, deals, and risks.
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Nadofaragene firadenovec-vncg Drug Asset Due Diligence Report 2026: Clinical, IP, Market, Deals, and Go/No-Go
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8 min read
Nadofaragene firadenovec-vncg Drug Asset Due Diligence Report 2026: Clinical, IP, Market, Deals, and Go/No-Go
21 July 2026
Nadofaragene firadenovec-vncg: Approved. 2026 diligence verdict: GO. Evidence review covers clinical, IP, deals, and risks.
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Tabelecleucel Drug Asset Due Diligence Report 2026: Clinical, IP, Market, Deals, and Go/No-Go
Latest Hotspot
8 min read
Tabelecleucel Drug Asset Due Diligence Report 2026: Clinical, IP, Market, Deals, and Go/No-Go
21 July 2026
Tabelecleucel: Approved. 2026 diligence verdict: GO. Evidence review covers clinical, IP, deals, and risks.
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