Trial · NCT07911748
A Study of MBS314 for Injection in Participants With Relapsed/Refractory Multiple Myeloma.
NCT07911748, Phase 1, Phase 2, Not yet recruiting, Beijing Mabworks Biotech Co., Ltd.
3 sourcestrials-2026-11-12-0.4.0
Cite this record
ConductScience Library. A Study of MBS314 for Injection in Participants With Relapsed/Refractory Multiple Myeloma. Trials, record NCT07911748. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07911748
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- A Study of MBS314 for Injection in Participants With Relapsed/Refractory Multiple Myeloma.
- NCT number
- NCT07911748
- Status
- Not yet recruiting
- Phases
- Phase 1, Phase 2
- Enrollment
- 78 participants, estimated
- Lead sponsor
- Beijing Mabworks Biotech Co., Ltd.
- Conditions
- Multiple Myeloma
- Interventions
- MBS314 for Injection
- First posted
- 2026-11-03
- Last updated
- 2026-11-04
Source ClinicalTrials.gov
Registered outcomes5
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Phase I ：Percentage of Participants with Adverse Events (AEs) | From Baseline up to 28 (+7) days after the last dose of MBS314] | Percentage of Participants with AEs and SAEs Assessed by NCI CTCAE v6.0. |
| Primary | Phase I：Incidence of Dose Limiting Toxicities (DLTs) | From Baseline up to 4 weeks | |
| Primary | Phase I：Maximum Tolerated Dose (MTD) (if any) or Optimal Biological Dose (OBD) of MBS314 | Up to approximately 7 months | |
| Primary | Phase I：Recommended Phase Ⅱ Dose (RP2D) of MBS314 | Up to approximately 7 months | |
| Primary | Phase II：Efficacy: Overall Response Rate (ORR) as Assessed by the Investigator | Up to approximately 15 months | ORR is defined as the proportion of participants who achieve sCR, CR, VGPR or PR according to the 2016 IMWG response criteria, as assessed by the investigator. |
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.
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.
Source
- Release
- trials-2026-11-12-0.4.0
- Release manifest SHA-256
- 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
- Registry capture
- 2026-11-12
- Results copy, AACT
- 2026-03-23
- NIH clinical studies file
- 2026-11-13
Source ClinicalTrials.gov
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNone 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/NCT07911748
GET https://conductscience.org/api/trials/v1/NCT07911748/registered