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Study identifier: NCT05357651 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Study to Assess the Safety and Efficacy of LB1410 in Participants With Advanced Solid Tumor or Lymphoma(Keyplus-001)

Condition: Solid Tumor · Lymphoma  ·  Sponsor: L & L Bio Co., Ltd., Ningbo, China

PhasePhase 1
Planned participants100
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a Phase I study designed to evaluate if experimental anti-PD-1 and anti-TIM-3 bispecific antibody, LB1410, is safe, tolerable and efficacious in participants with advanced solid tumors or lymphoma.

This description comes directly from the study's public registry record.

Talk to the study team

Yan Luan  ·  +86-21-54152522  ·  luanyn2@lnlbio.com

Always discuss trial participation with your own doctor first.

Locations (1)

Shanghai Pulmonary HospitalShanghai, Shanghai Municipality, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT05357651