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Atherosclerotic Vascular Disease

0 original drugs
0
Novel Drugs
1
Reformulations
0
Active Trials
1
Drug Targets

Atherosclerotic Vascular Disease has 0 FDA-approved novel treatments across 1 drug target. Explore market leaders, treatments by mechanism, the clinical pipeline, and drug targets below.

Phase 3 Readouts Pro

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

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Q4 2026
Obicetrapib
NewAmsterdam Pharma
Estimated · stale NCT05202509
Q4 2027
Inclisiran sodium 300 mg
Novartis
Estimated · fresh NCT05030428
Q1 2028
Pelacarsen
Novartis
Estimated · fresh NCT06813911
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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.

Atherosclerotic Vascular Disease Treatments by Mechanism

Top 4 mechanisms across 8 industry trials with a known mechanism of action.

See full pipeline →
Adenosine Triphosphate-Citrate Lyase Inhibitor
5 trials 2 sponsors
Microtubule Inhibitor
1 trials 1 sponsor
PCSK9 Inhibitor
1 trials 1 sponsor
IL1R1
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.

Atherosclerotic Vascular Disease Clinical Pipeline by Phase

100 industry-sponsored trials across 42 sponsors

Novel Atherosclerotic Vascular Disease Drugs by Company (New molecular entities)

No novel drugs found for this indication.

Reformulations (1 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.

Atherosclerotic Vascular Disease Drug Targets

Molecular targets of approved and investigational Atherosclerotic Vascular Disease drugs — 1 target tracked.

Generic Drugs (9 ANDA approved) Click to expand

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