TC-5214 as Augmentation Therapy in Patients With Refractory Hypertension
Study Details
Study Description
Brief Summary
A pilot study of subjects with refractory hypertension (on 3 concomitant agents with SBP > 140 mmHg and a DBP > 90 mmHg) randomized in a double-blind fashion to receive 4 single escalating doses of study medication in clinic.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 1/Phase 2 |
Detailed Description
12 subjects with refractory hypertension will be randomized in a double-blind fashion to receive single escalating doses of study medication in-clinic: on Day 1 (1mg), Day 8 (2mg), Day 15 (4mg) and Day 22 (8mg). On each of these 4 days, 10 subjects will receive TC-5214, and 2 subjects will receive placebo. Placebo treatments will be pooled across the 4 days of single-dose to produce an equivalent reference cohort (n = 8) for each treatment dose (n=10). Following the single-dose administration of 8mg in the clinic on Day 22, subjects will continue with two weeks (Days 23 - 35) of outpatient self-administration of TC-5214 (4mg BID; n = 6), or matching placebo (BID; n = 6). On Day 36, subjects will return for a final in-clinic dose of either TC-5214 (4mg, n = 6) or placebo (n = 6). There will be a 1-week follow-up period at the end of the treatment period.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Placebo Comparator: Placebo Subjects may receive a single, oral dose of placebo (capsule) in one of 4 crossover periods. Also, subjects may receive placebo orally, twice daily for 14 days in the last phase of the study. |
Drug: Placebo
Matching placebo
|
| Experimental: 1 mg TC-5214 Subjects may receive a single, oral capsule of 1 mg TC-5214 in one of 4 crossover periods. |
Drug: TC-5214
|
| Experimental: 2 mg TC-5214 Subjects may receive a single, oral capsule of 2 mg TC-5214 in one of 4 crossover periods. |
Drug: TC-5214
|
| Experimental: 4 mg TC-5214 Subjects may receive a single, oral capsule of 4 mg TC-5214 in one of 4 crossover periods. Also, subjects may receive 4 mg TC-5214 orally, twice daily for 14 days in the last phase of the study. |
Drug: TC-5214
|
| Experimental: 8 mg TC-5214 Subjects may receive a single, oral capsule of 8 mg TC-5214 in one of 4 crossover periods. |
Drug: TC-5214
|
Outcome Measures
Primary Outcome Measures
- Mean difference between TC-5214 and placebo in change at 3 hours from baseline SBP [Following dosing, 3 manual seated BP measurements and orthostatic BP measurements will be obtained in an identical fashion, at 30 minutes post-dose and at 1, 2, 3, 4, 5, 6, 7, and 8 hrs post-dose.]
Secondary Outcome Measures
- Safety and tolerability of TC-5214 in patients with refractory hypertension and obtain preliminary dose-response estimates [Days 1, 8, 15, 22 and 36]
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Refractory hypertension, defined as a SBP of >140mmHg and a DBP > 90mmHg, on stable doses of at least 3 concomitant antihypertensive treatment (which must include a diuretic and an ACEI, ARB or RA) for 8 weeks prior to Screening. All approved antihypertensive treatments are allowed except for alpha-adrenergic blockers, hydralazine, clonidine, guanethidine, guanadrel, and rauwolfia alkaloids.
-
Stable hypertension, as defined by: a. mean SBP on Day -7 that is within 20mmHg of the mean SBP on Day 1, with both mean SBPs > 140mmHg; and b. mean DBP on Day -7 that is within 10mm of the mean DBP on Day 1, with both mean DBPs > 90mmHg.
-
Outpatient with stable housing.
-
Subjects must be able to stay in the clinic for 8 hrs on Day 1, Day 8, Day 15, Day 22, and Day 36.
-
Able to give and to sign informed consent.
Exclusion Criteria:
-
Any unstable medical condition other than hypertension;
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Stage 3 hypertension (SBP > 180mmHg and/or DBP > 110mmHg);
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Heart rate > 100 beats per minute;
-
WOCBP who is pregnant or who is planning to become pregnant during the study;
-
History within past year of alcohol or illicit drug abuse;
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Unable to comply with study procedures in opinion of investigator;
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Concomitant medications for any medical condition that is uncontrolled for more than 2 weeks prior to study entry;
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Current use of alpha-adrenergic blocker, hydralazine, clonidine, guanethidine, guanadrel, or rauwolfia alkaloids;
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History of myocardial infarction or angina pectoris;
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Current seizure disorder;
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Renal insufficiency as defined by a serum creatinine > 2.0;
-
Uncontrolled hypothyroidism, vitamin B12 or folic acid deficiency;
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History of or concurrent ileus, glaucoma, or urinary retention;
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Inability of subject to understand and sign the ICF;
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Known systemic infection (HBV, HCV, HIV, TB);
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Current use of smoking cessation therapy within 4 weeks of screening;
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Use of herbal supplements;
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Clinically significant finding on physical exam;
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Clinically significant laboratory or ECG abnormality, including QTcF > 460 msec;
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Participation in another clinical trial in last month;
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Body Mass Index (BMI) > 35.
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Body weight < 100 pounds.
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Site staff or family member of study site staff.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Piedmont Medical Research | Winston-Salem | North Carolina | United States | 27101 |
Sponsors and Collaborators
- Targacept Inc.
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- TC-5214-23-CRD-002