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Life Sciences Intelligence · 2026
 
Oligonucleotide Therapeutics:
Uncovering the Next Platform and Market Shift  

Two reports. One competitive picture of the oligonucleotide market through the 2027-2036 expiry wave.
  • - Patent Intelligence: who owns the freedom to operate, and where the platform race is headed next.
  • - Clinical & Commercial Intelligence: who's leading the pipeline, and who's positioned to win in the clinic.

 
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📄 What's inside
 

As oligonucleotides move beyond rare disease into common indications, two forces are deciding who wins: platform IP across chemistry, delivery, and the 2027-2036 expiry wave, and market execution across trials, sponsors, and licensing.

 
Part 1 · Patent intelligence

What patent intelligence reveals about the next wave of platform competition

1
From composition-of-matter to platform control

Why a single sequence patent no longer explains an estate built on delivery, conjugation and process claims.

2
The stack beneath the sequence

Where chemistry and manufacturing innovation is concentrating, and why extrahepatic delivery is the biggest whitespace left.

3
The 2027-2036 expiry wave

What the patent cliff opens up, a watchlist of assets to track, and how China-based filers are moving on the same technologies.

Part 2 · Clinical & commercial intelligence

What clinical and commercial intelligence reveals about the next phase of market competition

1
Where modality momentum is shifting

682 trials by modality: ASO leads the pipeline at 313, but CRISPR has overtaken siRNA on new-trial count.

2
Where capital is flowing

A year of deals by structure, stage and therapeutic area, and who is buying versus originating.

3
Four signals to watch

Delivery beyond the liver, manufacturing as a strategic constraint, and China as both market and early signal.

What the data shows

682

Trials analysed, 2017-2026. CRISPR has already overtaken siRNA on new-trial starts.

Is your competitive map still ranking modalities by yesterday's leader?
2,545

Patent records expiring 2027-2036, mapped to the assignees holding them.

The whitespace opens on a schedule. Part 1 names the assets and the dates.
26

Approved drugs across ASO, siRNA, aptamer and CRISPR. The modality is no longer a rare-disease niche.

So who owns the patents behind them, and when do those patents lapse?
📅Deal timeline · May 2025 to May 2026

Every move that mattered, month over month

Twelve months of licences, collaborations and acquisitions, tracked in Synapse. Capital is following validated assets, delivery technology and tissue access.

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Through connected datasets across IP, drug discovery, clinical through to commercial areas, together with the proprietary AI and pharma-trained GPT, Synapse helps Therapeutic, Search & Evaluation and Competitive Intelligence leads to extrapolate unparalleled intelligence to make informed decisions to drive R&D and clinical investments with confidence.
  •  
    - Normalize the noise: Standardized drug-disease-target ontologies for precise analysis.
  •  - Break down silos: All-in-one platform for R&D, IP, CI and BD teams to accelerate decisions.
  •  - Surface early signals: Monitor early-stage assets and global competitive shifts in real-time.
  •  - Invest with certainty: Seamlessly connect patent, clinical, drug, and deal data to de-risk every investment.