Trial · NCT07009457
A Clinical Study of SHR-1316 (SC) Combined With Carboplatin and Etoposide as First-line Treatment for Extensive Stage Small Cell Lung Cancer
NCT07009457, Phase 1, Active not recruiting, Suzhou Suncadia Biopharmaceuticals Co., Ltd.
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. A Clinical Study of SHR-1316 (SC) Combined With Carboplatin and Etoposide as First-line Treatment for Extensive Stage Small Cell Lung Cancer. Trials, record NCT07009457. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07009457
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- A Clinical Study of SHR-1316 (SC) Combined With Carboplatin and Etoposide as First-line Treatment for Extensive Stage Small Cell Lung Cancer
- NCT number
- NCT07009457
- Status
- Active not recruiting
- Phases
- Phase 1
- Enrollment
- 24 participants, actual
- Lead sponsor
- Suzhou Suncadia Biopharmaceuticals Co., Ltd.
- Conditions
- Widespread Small Cell Lung Cancer
- Interventions
- SHR-1316 (sc) Injection, SHR-1316 Injection, Carboplatin Injection, Etoposide Injection
- First posted
- 2025-06-06
- Last updated
- 2026-06-30
Source ClinicalTrials.gov
Registered outcomes12
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | SHR-1316 serum trough concentration (Ctrough) | Day1 pre-dose to Day28. | |
| Primary | Area under the concentration curve from time 0 to 21 days for SHR-1316 (sc) (AUC0-21d) | Day1 pre-dose to Day21. | |
| Primary | Area under the concentration curve from time 0 to 28 days for SHR-1316 (sc) (AUC0-28d) | Day1 pre-dose to Day28. | |
| Secondary | Maximum Concentration of SHR-1316 (sc) (Cmax) | Day1 pre-dose to Day28. | |
| Secondary | Time to maximum plasma concentration (Tmax) | Day1 pre-dose to Day28. | |
| Secondary | Terminal half-life (t1/2) | Day1 pre-dose to Day28. | |
| Secondary | Incidence and severity of adverse events (AEs) | About 2 years. | |
| Secondary | Objective Response Rate (ORR) | About 2 years. | |
| Secondary | Duration of Relief (DoR) | About 1.5 years. | |
| Secondary | Disease Control Rate (DCR) | About 2 years. |
1 to 10 of 12Source ClinicalTrials.gov
See all 12 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/NCT07009457
GET https://conductscience.org/api/trials/v1/NCT07009457/registered