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Asset / Drug

Lenalidomide

Drug and asset intelligence for Lenalidomide with 16 indexed intelligence signals across regulatory, clinical, competitive, and market developments.

Signals
10
Catalysts
6
Stage
Development stage unavailable

Sponsor company

Lupin →

Mechanism of action

Chemotherapy

Recent signals(10)

ClinicalAugust 17, 2026

Phase II Trial of Brentuximab Vedotin and Lenalidomide in Relapsed/Refractory T-Cell Lymphoma

A phase II trial is underway to evaluate the efficacy of brentuximab vedotin combined with lenalidomide in patients with stage IB-IVB relapsed or refractory T-cell lymphoma.

ClinicalAugust 15, 2026

Study on Belantamab Mafodotin and Lenalidomide in Newly Diagnosed Multiple Myeloma

A clinical trial is underway to evaluate the efficacy of belantamab mafodotin combined with lenalidomide as maintenance therapy in newly diagnosed multiple myeloma patients post-autologous hematopoietic cell transplantation.

StrategyJuly 31, 2026

FDA Approves Lenalidomide ANDA217554 Submission by Deva Holding AS

The FDA has approved the ANDA217554 submission for Lenalidomide by Deva Holding AS.

RegulatoryJuly 30, 2026

FDA Accepts Supplement Application for Lenalidomide by Arrow International

The FDA has accepted a supplemental application for lenalidomide submitted by Arrow International.

ClinicalJuly 26, 2026

Lenalidomide being studied for treatment of adult histiocyte disorders

A clinical trial is investigating Lenalidomide for treating Langerhans cell histiocytosis, Erdheim-Chester disease, and histiocytic sarcoma.

RegulatoryJuly 7, 2026

FDA Accepts Supplement for Lenalidomide by Biocon Pharma

The FDA has accepted a supplemental application for Lenalidomide submitted by Biocon Pharma.

RegulatoryJuly 7, 2026

FDA Accepts Supplement Application for Lenalidomide by Accord Healthcare

The FDA has accepted a supplemental application for Lenalidomide submitted by Accord Healthcare.

RegulatoryJuly 6, 2026

FDA Accepts Supplement Application for Lenalidomide by QILU

The FDA has accepted a supplemental application for Lenalidomide submitted by QILU.

RegulatoryJuly 6, 2026

FDA Acceptance of Lenalidomide Supplement Application by Mylan

The FDA has accepted Mylan's supplemental application for Lenalidomide under ANDA213912.

StrategyJuly 6, 2026

Lupin's Lenalidomide ANDA214398 Receives Abbreviated Approval

Lupin has received abbreviated approval for its ANDA214398 application for Lenalidomide.

Upcoming milestones

No catalysts indexed for this entity yet.

Related catalysts(6)

Topline Data

— Lenalidomide

July 7, 2026 · N/A

Topline Data

— Lenalidomide

July 7, 2026 · N/A

Topline Data

— Lenalidomide

July 7, 2026 · N/A

Topline Data

— Lenalidomide

July 6, 2026 · N/A

Topline Data

— Lenalidomide

July 6, 2026 · N/A

Topline Data

— Lenalidomide

July 6, 2026 · N/A

Indications

T-Cell Lymphoma →

Therapeutic areas

Chemotherapy →
Hematology →
Immunomodulator →
Multiple Myeloma →
Oncology →
Oncology · Immunomodulator →
Oncology · Multiple Myeloma →
Oncology · Small Molecule →
Small Molecule →
T-Cell Lymphoma →

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