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Sativex

Jazz Pharmaceuticals · FDA-approved active Small molecule Under review Quality 9/100

Sativex is a Small molecule drug developed by Jazz Pharmaceuticals. It is currently FDA-approved for Muscle Spasticity due to Multiple Sclerosis. Also known as: Nabiximols, GW1000-02, THC/CBD spray, GW-1000-02.

Sativex, also known as nabiximols, is a botanical drug approved in the UK in 2010 as a mouth spray for the treatment of multiple sclerosis symptoms, including neuropathic pain, spasticity, and overactive bladder. It is a small molecule modality that contains a cannabis extract, specifically a THC-dominant cannabis formulation.

At a glance

Generic nameSativex
Also known asNabiximols, GW1000-02, THC/CBD spray, GW-1000-02, THC:CBD spray
SponsorJazz Pharmaceuticals
ModalitySmall molecule
Therapeutic areaNeuroscience
PhaseFDA-approved

Approved indications

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

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

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Frequently asked questions about Sativex

What is Sativex?

Sativex is a Small molecule drug developed by Jazz Pharmaceuticals, indicated for Muscle Spasticity due to Multiple Sclerosis.

What is Sativex used for?

Sativex is indicated for Muscle Spasticity due to Multiple Sclerosis.

Who makes Sativex?

Sativex is developed and marketed by Jazz Pharmaceuticals (see full Jazz Pharmaceuticals pipeline at /company/jazz-pharmaceuticals).

Is Sativex also known as anything else?

Sativex is also known as Nabiximols, GW1000-02, THC/CBD spray, GW-1000-02, THC:CBD spray.

What development phase is Sativex in?

Sativex is FDA-approved (marketed).

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing