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NCT05474885UNKNOWNanonymous

BCMA-CD19 cCAR T Cell Treatment of Relapsed/Refractory Systemic Lupus Erythematosus (SLE)

Sponsor

Source record

iCell Gene Therapeutics

Phase

Source record

Phase 1

Modality

AI-normalized

protein therapy

Target

AI-normalized

BCMA-CD19 chimeric antigen receptor (cCAR) targeting B cells and plasma cells involved in systemic lupus erythematosus (SLE).

Indication / condition

AI-normalized

Relapsed/Refractory, Systemic Lupus Erythematosus (SLE)

Intervention

Source record

BCMA-CD19 cCAR T cells

Source & freshness

Source record

NCT ID

NCT05474885

Original source

ClinicalTrials.gov

Source last updated

Jul 26, 2022

Ingested at

Jun 13, 2026

Internal sync

Jun 13, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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NCT ID

NCT05474885

Title

BCMA-CD19 cCAR T Cell Treatment of Relapsed/Refractory Systemic Lupus Erythematosus (SLE)

Sponsor

iCell Gene Therapeutics

Status

UNKNOWN

Phase

Phase 1

Condition raw

Relapsed/Refractory, Systemic Lupus Erythematosus (SLE)

Condition normalized

Relapsed/Refractory, Systemic Lupus Erythematosus (SLE)

Modality raw

protein therapy

Modality normalized

protein therapy

Target raw

BCMA-CD19 chimeric antigen receptor (cCAR) targeting B cells and plasma cells involved in systemic lupus erythematosus (SLE).

Target normalized

BCMA-CD19 chimeric antigen receptor (cCAR) targeting B cells and plasma cells involved in systemic lupus erythematosus (SLE).

Interventions

BCMA-CD19 cCAR T cells

Public preview

Source record

The BCMA-CD19 cCAR T cell therapy, sponsored by iCell Gene Therapeutics, aims to address relapsed/refractory systemic lupus erythematosus (SLE), a chronic autoimmune disease with significant unmet medical needs. Current treatments primarily focus on symptom management rather than disease modification. The potential to deplete pathogenic B cells and plasma cells positions this therapy uniquely in the market, which is currently dominated by biologics like rituximab and belimumab. The trial's success could lead to a novel treatment paradigm, enhancing iCell's competitive edge in the immunotherapy space. However, the market landscape is competitive, with several other CAR T cell therapies and biologics under development for autoimmune disorders. Diligence is required to assess regulatory pathways and potential market access challenges, particularly in the context of safety and efficacy data from ongoing trials.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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