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NCT04824092PHASE3ACTIVE_NOT_RECRUITING2 endpoints open for prediction

Tafasitamab + Lenalidomide + R-CHOP Versus R-CHOP in Newly Diagnosed High-intermediate and High Risk DLBCL Patients

A Phase 3, Multicenter, Randomized, Double-blind, Placebo-controlled Trial Comparing the Efficacy and Safety of Tafasitamab Plus Lenalidomide in Addition to R-CHOP Versus R-CHOP in Previously Untreated, High-intermediate and High-risk Patients With Newly-diagnosed Diffuse Large B-cell Lymphoma (DLBCL)

Sponsor: Incyte Corporation

Open for Predictions · 2 endpoints

NCT04824092Hazard Ratio for Event-Free Survival (EFS)Primary

AA Hazard Ratio below 1.0 favours tafasitamab + lenalidomide + R-CHOP. The primary endpoint of FRONTMIND. Toplined positive January 2026 — full HR data at ASCO 2026 LBA7000.

Prediction range: 0.40.9 Hazard Ratio
NCT04824092Hazard Ratio for Overall Survival (OS)

A Hazard Ratio below 1.0 favours the treatment arm. HR 0.75 means a 25% reduction in the risk of death.

Prediction range: 0.41.2 Hazard Ratio

Key Facts

Study type
INTERVENTIONAL
Conditions
Diffuse Large B-cell Lymphoma
Interventions
Tafasitamab, Lenalidomide, Rituximab, Cyclophosphamide
Enrollment
899 participants
Primary completion
Sep 2026
Study completion
Nov 2027
First posted
Apr 2021
Last updated
Apr 2026

Primary Endpoints (CT.gov)

PFS-INV

Time frame: Time from date of randomization until Progressive Disease or death from any cause. In this trial, the primary endpoint is PFS as assessed by the investigator (up to 43 months)

Secondary Endpoints

EFS-INV

OS

Metabolic PET-negative CR-rate at EOT by BIRC

Eligibility Criteria

Major Inclusion Criteria: * Previously untreated patients with local biopsy-proven, CD20-positive DLBCL, including one of the following diagnoses by 2016 World Health Organization (WHO) classification of lymphoid neoplasms are eligible: 1. DLBCL, NOS including GCB type, ABC type 2. T-cell rich large BCL 3. Epstein-Barr virus-positive DLBCL, NOS 4. Anaplastic lymphoma kinase (ALK)-positive large BCL 5. Human herpes virus-8 (HHV8)-positive DLBCL, NOS 6. High-grade BCL with MYC and B-cell lymphoma 2 (BCL2) and/or B-cell lymphoma 6 (BCL6) rearrangements (double-hit or triple-hit lymphoma). Please note: Patients must be appropriate candidates for R-CHOP. If an investigator deems a patient with a known double- or triple-hit lymphoma (HGBL) should be treated more aggressively (e.g. dose-adjusted etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin and rituximab \[DA-EPOCH-R\] or cyclophosphamide, vincristine, doxorubicin and dexamethasone (CVAD) followed by methotre

Read full criteria on CT.gov →

✦ Analyst Commentary

Expert commentary on why this trial matters and what to watch for.

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Source

Open on ClinicalTrials.gov

Related Program

Monjuvi (tafasitamab)

Incyte / MorphoSys

View program page →