Trial · NCT07905560
A Study of Safety of SUN-0864 and How it is Processed by and Affects the Body in Healthy Adults and Healthy Adults Who Are Overweight or Obese.
NCT07905560, Phase 1, Not yet recruiting, Superluminal Medicines, Inc.
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. A Study of Safety of SUN-0864 and How it is Processed by and Affects the Body in Healthy Adults and Healthy Adults Who Are Overweight or Obese. Trials, record NCT07905560. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07905560
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- A Study of Safety of SUN-0864 and How it is Processed by and Affects the Body in Healthy Adults and Healthy Adults Who Are Overweight or Obese.
- NCT number
- NCT07905560
- Status
- Not yet recruiting
- Phases
- Phase 1
- Enrollment
- 138 participants, estimated
- Lead sponsor
- Superluminal Medicines, Inc.
- Conditions
- Healthy Participants
- Interventions
- SUN-0864 or placebo, SUN-0864 or placebo, SUN-0864 or placebo, SUN-0864 (Formulation 1) or SUN-0864 (Formulation 2), Placebo
- First posted
- 2026-10-29
- Last updated
- 2026-10-29
Source ClinicalTrials.gov
Registered outcomes15
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Number of Participants With Treatment Emergent Treatment-Related Adverse Event(s) (Treatment-Related TEAE) (Part 1) | Baseline up to Follow-Up (From Day -28 (Screening) to Day 37 (FUP visit) | |
| Primary | Number of Participants With Treatment Emergent Treatment-Related Adverse Event(s) (Treatment-Related TEAE) (Part 2) | From Day -28 (Screening) to Day 60 (FUP visit) | |
| Primary | Number of Participants With Treatment Emergent Treatment-Related Adverse Event(s) (Treatment-Related TEAE) (Part 3) | From Day -28 (Screening) to Day 119 (FUP visit) | |
| Primary | Number of Participants With Treatment Emergent Treatment-Related Adverse Event(s) (Treatment-Related TEAE) (Part 4) | From Day -28 (Screening) to Day 37 (FUP visit) | |
| Primary | Cmax measurement of SUN-0864 in Part 4 | up to 48 hours post-dose. Daily from Day 1 (Predose) to Day 3. | |
| Primary | Tmax measurement of SUN-0864 in Part 4 | up to 48 hours post-dose. Daily from Day 1 (Predose) to Day 3. | |
| Primary | t1/2 measurement of SUN-0864 in Part 4 | up to 48 hours post-dose. Daily from Day 1 (Predose) to Day 3. | |
| Primary | AUClast measurement of SUN-0864 in Part 4 | up to 48 hours post-dose. Daily from Day 1 (Predose) to Day 3. | |
| Primary | AUCinf measurement of SUN-0864 in Part 4 | up to 48 hours post-dose. Daily from Day 1 (Predose) to Day 3. | |
| Primary | AUC24 measurement of SUN-0864 in Part 4 | up to 24 hours post-dose. Daily from Day 1 (Predose) to Day 3. |
1 to 10 of 15Source ClinicalTrials.gov
See all 15 registered outcomesOutcomes0
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.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
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/NCT07905560
GET https://conductscience.org/api/trials/v1/NCT07905560/registered