Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

High Risk

Score: 60/100

Failure Rate

46.2%

6 terminated/withdrawn out of 13 trials

Success Rate

50.0%

-36.5% vs industry average

Late-Stage Pipeline

31%

4 trials in Phase 3/4

Results Transparency

100%

6 of 6 completed trials have results

Key Signals

1 recruiting6 with results

Enrollment Performance

Analytics

Phase 2
5(38.5%)
Phase 1
4(30.8%)
Phase 3
4(30.8%)
13Total
Phase 2(5)
Phase 1(4)
Phase 3(4)

Activity Timeline

Global Presence

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Clinical Trials (13)

Showing 13 of 13 trials
NCT03848481Phase 2Terminated

CBDV vs Placebo in Children and Adults up to Age 30 With Prader-Willi Syndrome (PWS)

Role: collaborator

NCT03202303Phase 2Recruiting

Cannabidivarin (CBDV) vs. Placebo in Children With Autism Spectrum Disorder (ASD)

Role: collaborator

NCT04252586Phase 3Terminated

A Long-term Safety Study of Cannabidiol Oral Solution (GWP42003-P, CBD-OS) in Patients With Rett Syndrome

Role: collaborator

NCT02544750Phase 3Completed

An Open-label Extension Trial of Cannabidiol (GWP42003-P, CBD) for Seizures in Tuberous Sclerosis Complex (GWPCARE6)

Role: collaborator

NCT04423341Phase 2Completed

Effect of Non-psychoactive Cannabidiol as an Adjunct to Botulinum Toxin in Blepharospasm

Role: collaborator

NCT02240160Phase 1Terminated

A Randomised, Open-label, Three-way Crossover Study to Assess the Pharmacokinetics and Safety of Single Doses of Four Sprays of Sativex® in a Range of Oral pH Environments in Healthy Subjects

Role: lead

NCT01262651Phase 3Completed

Sativex® for Relieving Persistent Pain in Participants With Advanced Cancer

Role: lead

NCT02325024Phase 1Withdrawn

A Study to Evaluate the Pharmacokinetics Of Sativex® in Subjects With Severe Renal Impairment or End Stage Renal Disease, Compared to Matched Subjects With Normal Renal Function.

Role: lead

NCT01975688Phase 1Terminated

A Pharmacokinetic Study of Single Doses of Sativex in Treatment-induced Mucositis

Role: lead

NCT02432612Phase 1Withdrawn

A Study to Assess the Pharmacokinetic (PK) Properties of Sativex® in Patients With Advanced Cancer

Role: lead

NCT00391079Phase 3Completed

Sativex Versus Placebo When Added to Existing Treatment for Central Neuropathic Pain in MS

Role: lead

NCT00530764Phase 2Completed

A Study of Sativex® for Pain Relief in Patients With Advanced Malignancy.

Role: lead

NCT01502046Phase 2Completed

Neuroprotection by Cannabinoids in Huntington's Disease

Role: collaborator

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