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Multiple Sclerosis

CNS 9 original drugs
9
Novel Drugs
7
Reformulations
182
Active Trials
17
Drug Targets

Phase 3 Readouts Pro

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

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Q4 2026
CYB704
Novartis
Estimated · fresh NCT06847724
Q4 2026
Ocrelizumab
Roche
Estimated · fresh NCT03523858
Q4 2026
IMU-838 tablets
Immunic AG
Estimated · fresh NCT05134441
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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 12 mechanisms across 104 industry trials with a known mechanism of action.

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CD20-directed Cytolytic Antibody
31 trials 11 active 2 sponsors
Kinase Inhibitor
3 trials 2 active 2 sponsors
Interferon beta
12 trials 1 active 5 sponsors
Nicotinic acid receptor/Nrf2
25 trials 2 sponsors
Integrin Receptor Antagonist
11 trials 1 sponsor
Pyrimidine Synthesis Inhibitor
9 trials 3 sponsors
Sphingosine 1-phosphate Receptor Modulator
4 trials 2 sponsors
Purine Antimetabolite
4 trials 2 sponsors
CD52-directed Cytolytic Antibody
2 trials 2 sponsors
Muscarinic receptor
1 trials 1 sponsor
Benzodiazepine
1 trials 1 sponsor
Acetylcholine Release 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

476 industry-sponsored trials across 117 sponsors

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Reformulations (7 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 (8 ANDA approved) Click to expand

Related Indications

Other CNS 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