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Tramadol; JNS013

Phase 2

Osteoarthritis | Small molecule | Musculoskeletal |Johnson & Johnson|Last Updated: May 17, 2011

Target and mechanism

ModalitySmall molecule

Also known as Tramadol Hydrochloride; JNS013

Success Probability

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Market & Valuation

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Trial Design

UNCONTROLLED
Total Trials1
Total Enrollment119

FDA Designations

No designations recorded

Clinical trial landscape

Tramadol; JNS013 · 1 trial · 2 indications

Phase 2 1
NCT00752661An Exploratory Study of Tramadol Hydrochloride in Patients With Osteoarthritis of the Knee or Low Back PainOsteoarthritis
COMPLETED119 Analytics
PHASE2COMPLETED
An Exploratory Study of Tramadol Hydrochloride in Patients With Osteoarthritis of the Knee or Low Back Pain
OsteoarthritisUnlock trial analytics

Study Endpoints

Primary Endpoints

Change in the intensity of pain from the beginning of dose-finding period (baseline) to the final assessment point, by using VAS.

Secondary Endpoints

Percentage of patients considered analgesic effect present based on the change in VAS, VAS on each assessment day, PI (pain intensity rating), PAR (pain relief rating), PID (pain intensity difference), PRID (pain relief combined with pain intensity).
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Study Design & Arms

AllocationNON_RANDOMIZED
MaskingNONE
ModelSINGLE_GROUP
PurposeTREATMENT

Interventions

NameTypeDescription
Tramadol Hydrochloride; JNS013DRUG -
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Eligibility Criteria

Age Range20 Years to 74 Years
SexALL
Healthy VolunteersNo

Inclusion Criteria: * Patients with chronic pain due to OA of the knee or LBP that persists for more than 3 months at the initiation of the observation period * Patients who received oral NSAIDs at a usual highest dose for at least 14 consecutive days during 3 months before the initiation of the ob...

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