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| ID | Type | Description | Link |
|---|---|---|---|
| 1UG3NS123965-01 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| National Institute of Neurological Disorders and Stroke (NINDS) | NIH |
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This clinical study is being conducted to evaluate the safety, tolerability, plasma pharmacokinetics and efficacy of an investigational drug called CNTX-3001. This Phase 1 study is the first time that CNTX-3001 will be given to people (first-in-human study). The study is being done to evaluate whether CNTX-3001, given into the intrathecal space by lumbar puncture, can be administered safely to participants who have been diagnosed with intractable chronic moderate to severe low back pain and who have not responded well to other treatments in the past.
CNTX-3001 is a novel, non-opioid small molecule
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| CNTX-3001 | Experimental | Single intrathecal injection of CNTX-3001 |
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| Placebo | Placebo Comparator | Single intrathecal injection of normal saline |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| CNTX-3001 | Drug | non-opioid analgesic |
| |
| Placebo |
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of treatment emergent adverse events | Number of participants with TEAEs, which includes laboratory test variables | From baseline to the end of treatment visit (Day 7) |
| Measure | Description | Time Frame |
|---|---|---|
| Maximum Observed Plasma Concentration (Cmax) of CNTX-3001 | Pre dose to up to 4 hours post dose | |
| Time to Maximum Observed Plasma Concentration (Tmax) of CNTX-3001 | Pre dose to up to 4 hours post dose |
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Inclusion:
Have stable intractable, chronic moderate to severe low back pain
Must have failed all 3 of the following categories of therapies:
If the intractable low back pain is accompanied by radicular pain, back pain must be dominant over leg pain and may not radiate below the knee
Has normal leg strength in both legs (able to stand/walk)
Willing and able to undergo the lumbar puncture
On a stable analgesic regimen, or a stable dose of an opioid medication for >3 months
Non- or ex-smoker and has not used any nicotine-containing products within 3 months
Men or women able to abide by reproductive and contraceptive requirements
Has a body mass index (BMI) between 18 and 35 kg/m2, with weight ≥60 kg
Exclusion
Exclusion
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Clinical Operations | Contact | (617) 837-6911 | clinicalops@centrexion.com |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Neurovations | Recruiting | Napa | California | 94558 | United States |
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| ID | Term |
|---|---|
| D017116 | Low Back Pain |
| ID | Term |
|---|---|
| D001416 | Back Pain |
| D010146 | Pain |
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
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| Drug |
Placebo product |
|
| Area Under the Concentration-time Curve up to the Last Measurable Concentration of CNTX-3001 | Pre dose to up to 4 hours post dose |
| D013568 |
| Pathological Conditions, Signs and Symptoms |