Trial · NCT07901413
Evaluation of ICP-B381 in Patients With Advanced Solid Tumors
NCT07901413, Phase 1, Phase 2, Not yet recruiting, Beijing InnoCare Pharma Tech Co., Ltd.
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Evaluation of ICP-B381 in Patients With Advanced Solid Tumors. Trials, record NCT07901413. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07901413
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Evaluation of ICP-B381 in Patients With Advanced Solid Tumors
- NCT number
- NCT07901413
- Status
- Not yet recruiting
- Phases
- Phase 1, Phase 2
- Enrollment
- 348 participants, estimated
- Lead sponsor
- Beijing InnoCare Pharma Tech Co., Ltd.
- Conditions
- Advanced Solid Tumor
- Interventions
- ICP-B381
- First posted
- 2026-10-28
- Last updated
- 2026-10-28
Source ClinicalTrials.gov
Registered outcomes27
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | The type, severity (assessed according to the National Cancer Institute Common Terminology Criteria for Adverse Events version 6.0 [NCI-CTCAE V6.0]), relationship to the investigational product, and incidence rate of adverse event (AE) and serious advers | 2 years | |
| Primary | The type, severity (assessed according to NCI-CTCAE V6.0), and incidence rate of dose limiting toxicity (DLT) | 2 years | |
| Primary | Single-agent Recommended Dose (RD) and/or Maximum Tolerated Dose (MTD) | 2 years | |
| Primary | Participants with prostate cancer: Prostate-specific antigen (PSA50) response rate evaluated by Investigator according to Prostate Cancer Working Group 3 (PCWG3) criteria | 2 years | |
| Primary | Participants with other tumor types: Investigator-assessed Objective response rate (ORR) according to Response Evaluation Criteria In Solid Tumors (RECIST) V1.1 criteria | 2 years | |
| Primary | The optimal dosing regimen for the subsequent study of ICP-B381 | 2 years | |
| Secondary | Maximum Concentration (Cmax) | 2 years | |
| Secondary | Time to Maximum Plasma Concentration (Tmax) | 2 years | |
| Secondary | Half-life (T1/2) | 2 years | |
| Secondary | Area Under the Serum or Plasma Concentration-Time Curve (AUC0-∞ and AUC0-t) | 2 years |
1 to 10 of 27Source ClinicalTrials.gov
See all 27 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/NCT07901413
GET https://conductscience.org/api/trials/v1/NCT07901413/registered?page=2