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SPM 962

Otsuka Pharmaceutical Co., Ltd. · Phase 3 active Small molecule

SPM 962 is a selective, high-affinity, and orally bioavailable small molecule inhibitor of the sphingosine-1-phosphate receptor 1 (S1PR1).

SPM 962 is a selective, high-affinity, and orally bioavailable small molecule inhibitor of the sphingosine-1-phosphate receptor 1 (S1PR1). Used for Relapsing forms of multiple sclerosis.

At a glance

Generic nameSPM 962
Also known asrotigotine
SponsorOtsuka Pharmaceutical Co., Ltd.
Drug classS1P receptor modulator
TargetS1PR1
ModalitySmall molecule
Therapeutic areaAutoimmune diseases
PhasePhase 3

Mechanism of action

By selectively inhibiting S1PR1, SPM 962 is expected to reduce the number of circulating lymphocytes, thereby reducing inflammation and potentially treating autoimmune diseases. This mechanism of action is distinct from other S1P receptor modulators, which often have a broader range of activity and may have different safety profiles.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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