A Clinical Trial of LBL-034 in Patients With Relapsed Refractory Multiple Myeloma
Combination regimen
A Multicenter, Open-label, Phase I/II Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of LBL-034 in Patients With Relapsed/Refractory Multiple Myeloma
Last checked 16 Oktober 2026Source ClinicalTrials.govNCT06049290Not verified
Four separate status dimensions
- RegistryRecruiting in registry
- SiteNot verifiedUnknown, so no conclusion can be drawn.
- International accessUnknownUnknown, so no conclusion can be drawn.
- Patient matchNot assessedUnknown, so no conclusion can be drawn.
Three statuses often treated as one
A recruiting registry status does not mean a patient can immediately join this study. These three questions are answered by different parties.
Registry status
Stated by the study record owner: whether the study is listed as recruiting. It does not state whether a site is active.
Site status
Stated by the facility: whether the site is running this study now. TanyaKanker has not verified this.
International access
Stated by facility policy: whether patients from outside the local country can be accepted.
Why this appears
Appears because it is recorded for Multiple Myeloma.
What to verify
- • Acceptance of patients from outside the local country has not been verified.
- • We have not verified that the study site is actively running this study.
- • Eligibility is determined by the study team, not by registry data.
- • This record has never been directly verified by us.
Preliminary screening only shows overlap and data needs. Eligibility is determined by the study team.
Why this study may be relevant
- This study is recorded for Multiple Myeloma, the same cancer group you are exploring.
- Recorded interventions: LBL-034 for Injection.
- The study is in Phase 1 / Phase 2 according to registry data.
- Locations are recorded in China.
The relevance above is assembled from registry data, not from an eligibility judgement.
Study basis
A Multicenter, Open-label, Phase I/II Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of LBL-034 in Patients With Relapsed/Refractory Multiple Myeloma
- Sponsor
- Nanjing Leads Biolabs Co.,Ltd
- Registry
- ClinicalTrials.gov NCT06049290
- Phase
- Phase 1 / Phase 2
Cancer and markers
Recorded interventions
Study locations
- China
The First Affiliated Hospital of Wannan Medical College
Wuhu
- China
Peking University People's Hospital
Beijing
- China
The First Affiliated Hospital of Xiamen University
Xiamen
- China
Sun Yat-sen University Cancer Center
Guangzhou
- China
Shenzhen Second People's Hospital
Shenzhen
Showing 5 of 21 locations recorded in the registry.
What we know
- Registry status: Recruiting.
- Phase 1 / Phase 2 with sponsor Nanjing Leads Biolabs Co.,Ltd.
- 21 locations recorded in the registry.
- Registry data updated 2026-09-11.
What we do not know yet
- Whether the site accepts patients from outside the local country.
- Whether the site is actively running the study now.
- Which cost components are borne by participants.
- Which documents the sponsor requires.
Main eligibility factors from the registry
- Protocol sex: all
- Protocol minimum age: 18 Years
- Complete eligibility criteria appear only in the study protocol and must be assessed by the study team.
This summary is taken from registry data. Complete criteria live in the study protocol and must be assessed by the study team.
Documents that may be needed
- Disease history summary from the treating doctor
- Most recent pathology report
- Molecular marker report if available
- Most recent imaging results
- List of current medicines
This is a general frame, not the sponsor's official list.
Updates and sources
- Registry update
- 2026-09-11
- Retrieved by TanyaKanker
- 2026-10-16
- Last verified
- Never
- Contact status
- Not contacted
Data comes from the public ClinicalTrials.gov registry of the US National Library of Medicine. Registry facts are public data; interpretation about international patient access, cost, and site readiness does NOT come from the registry and is marked unverified.
https://clinicaltrials.gov/study/NCT06049290Cost
NOT VERIFIED
Not verified. The public registry does not include cost details for international patients and does not state payment coverage.
This information is not a diagnosis or a medical recommendation. Decisions remain with your medical team.
Not a diagnosis and not final medical advice. Must be reviewed by a doctor.
Other studies in a similar group
AZD0120 in Relapsed/Refractory Multiple Myeloma (DURGA-1)
NCT05850234 | Phase 1 / Phase 2
A Study Comparing AZD0120, a Dual-targeted CAR-T Against B-cell Maturation Antigen (BCMA) and CD19, Versus Standard Regimens in Participants With Relapsed Refractory Multiple Myeloma (DURGA-4)
NCT07391657 | Phase 3
TAPUR: Testing the Use of Food and Drug Administration (FDA) Approved Drugs That Target a Specific Abnormality in a Tumor Gene in People With Advanced Stage Cancer
NCT02693535 | Phase 2
Safety and Efficacy of KSVCBD Injection in Multiple Myeloma Expressing CD19 and/or BCMA
NCT07620275 | Phase 1
Check preliminary match for your case
This screening shows overlap between your summary and the study, plus data that still needs to be completed. Eligibility remains the study team's decision.
After submission, a human navigator reviews your request and contacts you through your chosen channel. The WhatsApp message already includes this page context, so you do not need to explain from the beginning.
Clinical data is not requested in the form and is not sent to analytics. Do not send medical reports through WhatsApp or email; use the secure upload page. We do not promise eligibility or any treatment outcome.
Next steps
These suggestions come from links between entries in TanyaKanker's database, not from a medical judgement. Each suggestion includes why it appears.
To check
- Clinical trial document checklist
Tool
Reason: Check documents before contacting the study team
- Prepare questions for your doctor
Tool
Reason: Bring clear questions to the next conversation
What you can do
- Upload medical reports
Build a case summary in twelve steps
Reason: Often the most useful next step after reading this page
- Request a second opinion
Review of the treatment plan
Reason: Relevant when a treatment plan is being considered
- Consult a navigator
A request is recorded with this page context
Reason: For asking the next step directly
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