Trial · NCT06212648
Evaluate the Efficacy and Safety of SPC1001 and Monotherapy in Patients With Essential Hypertension
NCT06212648, Phase 2, Completed, Shin Poong Pharmaceutical Co. Ltd.
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Evaluate the Efficacy and Safety of SPC1001 and Monotherapy in Patients With Essential Hypertension. Trials, record NCT06212648. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06212648
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Evaluate the Efficacy and Safety of SPC1001 and Monotherapy in Patients With Essential Hypertension
- NCT number
- NCT06212648
- Status
- Completed
- Phases
- Phase 2
- Enrollment
- 253 participants, actual
- Lead sponsor
- Shin Poong Pharmaceutical Co. Ltd.
- Conditions
- Hypertension, Essential Hypertension
- Interventions
- SPC1001 High, SPC1001 Mid1, SPC1001 Mid2, SPC1001 Low, SPC3001, SPC4001, SPC4002, Placebo
- First posted
- 2024-01-19
- Last updated
- 2024-01-19
Source ClinicalTrials.gov
Registered outcomes5
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | MSSBP measures the amount of change after 8 weeks from baseline | 8 weeks from baseline | MSSBP measures the amount of change after 8 weeks from baseline |
| Secondary | MSSBP measures the amount of change after 4 weeks from baseline | 4 weeks from baseline | MSSBP measures the amount of change after 4 weeks from baseline |
| Secondary | MSDBP measures the amount of change after 4 weeks, 8 weeks from baseline | 4, 8 weeks from baseline | MSDBP measures the amount of change after 4 weeks, 8 weeks from baseline |
| Secondary | blood pressure normalization rate | 4, 8 weeks from baseline | The Proportion of subjects who reached target blood pressure at 4 and 8 weeks of administration of the clinical trial drug |
| Secondary | blood pressure response rate | 4, 8 weeks from baseline | The proportion of subjects whose MSSBP decreased by 20 mmHg or more and/or MSDBP decreased by 10 mmHg or more compared to baseline at 4 or 8 weeks after administration of the clinical trial drug |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 41162308 | DERIVED |
Source PubMed
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT06212648
GET https://conductscience.org/api/trials/v1/NCT06212648/registered