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Ankylosing Spondylitis

Immunology 17 original drugs
17
Novel Drugs
9
Reformulations
21
Active Trials
14
Drug Targets

Phase 3 Readouts Pro

6 active Phase 3 trials with confidence-graded completion dates.

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Q2 2026
Jaktinib
Suzhou Zelgen Biopharmaceuticals Co.,Ltd
Estimated · fresh NCT05861102
Q3 2026
Bimekizumab
UCB Biopharma SRL
Estimated · fresh NCT04436640
Q4 2026
LNK01001
Lynk Pharmaceuticals Co., Ltd
Estimated · fresh NCT07237568
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Anchored on CT.gov primary completion date. Topline announcements typically precede this by 3–9 months. Confidence labels combine date type (ACTUAL/ESTIMATED) with last-update freshness.

Treatments by Mechanism

Top 6 mechanisms across 18 industry trials with a known mechanism of action.

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Tumor Necrosis Factor Blocker
11 trials 7 sponsors
TNF
2 trials 1 sponsor
Interleukin-6 Receptor Antagonist
2 trials 1 sponsor
Interleukin-17A Antagonist
1 trials 1 sponsor
Nonsteroidal Anti-inflammatory Drug
1 trials 1 sponsor
Janus Kinase Inhibitor
1 trials 1 sponsor

MoA derived from FDA pharmClassEpc when intervention matches an approved drug. Codenamed clinical-stage assets without an approved counterpart show "—" and aren't grouped here — they're still in the phase tables below.

Clinical Pipeline by Phase

71 industry-sponsored trials across 40 sponsors

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Precision Medicine Biomarkers

All biomarkers →

Biomarkers used for patient selection in Ankylosing Spondylitis

Reformulations (9 drugs) Click to expand

Reformulations are FDA-approved versions of existing molecules in new dosage forms (e.g., oral solution vs tablet, extended-release vs immediate-release). They require a new NDA but use an already-proven active ingredient.

Generic Drugs (3 ANDA approved) Click to expand

Generic drugs contain the same active ingredient as the brand-name drug and are approved via ANDA (Abbreviated New Drug Application).

Related Indications

Other Immunology indications

Drug Categories:

  • Novel Drugs: NDA Type 1/2 (new molecular entity) or original BLA
  • Reformulations: NDA Type 3/5 (new dosage form of existing molecule)
  • Biosimilars: BLA-approved biologics highly similar to reference products
  • Generics: ANDA-approved copies of small molecule drugs

View data sources and methodology