Neoplasms

Blood and Lymph Conditions

Immune System Diseases

All Conditions

Rare Diseases

Lymphoma, Large B-Cell, Diffuse

Lymphoma

Lymphoma, B-Cell

Neoplasms by Histologic Type

Lymphoproliferative Disorders

Lymphatic Diseases

Immunoproliferative Disorders

Lymphoma, Non-Hodgkin

B-cell Lymphoma

Diffuse Large B-Cell Lymphoma

Lymphosarcoma

All Drugs and Chemicals

Antineoplastic Agents

Antibodies

Antibodies, Monoclonal

Lenalidomide

Immunoglobulins

Immunologic Factors

Angiogenesis Inhibitors

Growth Inhibitors

Tafasitamab plus lenalidomide in addition to R-CHOP

Six 21-day cycles of tafasitamab (12 mg/kg intravenously, on Day 1, 8 and 15) in addition to R-CHOP

Tafasitamab

Six 21-day cycles of tafasitamab (12 mg/kg intravenously, on Day 1, 8 and 15) plus lenalidomide (starting dose 25 mg orally, on Day 1-10) in addition to R-CHOP

Tafasitamab plus lenalidomide

Pia Kloepfer, MD

This is an open-label, randomized, multicentre study to evaluate safety and preliminary efficacy of the human anti-CD19 antibody Tafasitamab in addition to R-CHOP (Rituximab, Cyclophosphamide, Doxorubicin, Vincristin, Prednison) or Tafasitamab and Lenalidomide in addition to R-CHOP in adult patients with newly diagnosed, previously untreated Diffuse Large B-cell Lymphoma (DLBCL).

Phase Ib Study to Assess Safety and Preliminary Efficacy of Tafasitamab or Tafasitamab Plus Lenalidomide in Addition to R-CHOP in Patients With Newly Diagnosed DLBCL

A Phase Ib, Open-label, Randomized Study to Assess Safety and Preliminary Efficacy of Tafasitamab in Addition to R-CHOP or Tafasitamab Plus Lenalidomide in Addition to R-CHOP in Patients With Newly Diagnosed Diffuse Large B-Cell Lymphoma (DLBCL) - First-MIND

MorphoSys AG

intravenous Infusion of MOR00208, Fc-Optimized Anti-CD19 Antibody

MOR00208 (formerly Xmab 5574)

This is an open-label, multicenter study to characterize the safety and efficacy of the human anti-CD19 antibody MOR00208 in adult patients with relapsed/refractory non-Hodgkin's lymphoma (NHL) who have received at least 1 prior therapy containing rituximab (at least once).

The study enrols patients from four different NHL subtypes: follicular lymphoma (FL), diffuse large B-cell lymphoma (DLBCL), mantle cell lymphoma (MCL) and other indolent NHL (iNHL). The study will employ a two-stage design where the decision to further enrol any NHL subtype in stage 2 will depend on best responses after two or three cycles in stage 1.

Study of Fc-Optimized Anti-CD19 Antibody (MOR00208) to Treat Non-Hodgkin's Lymphoma (NHL)

A Phase IIa, Open-label, Multicenter Study of Single-agent MOR00208, an Fc-optimized Anti-CD19 Antibody, in Patients With Relapsed or Refractory B-Cell Non-Hodgkin's Lymphoma

Proportion of patients with Complete Remission (CR; disappearance of all evidence of disease) or Partial Remission (PR; regression of measurable disease and no new sites), assessed as per the 2007 International Working Group (IWG) response criteria by radiographic evaluations (CT, PET, MRI, or other).

Proportion of patients with Stable Disease (failure to attain CR/PR with no progressive disease)

Time from first CR or PR to first documentation of relapse/progression (any new lesion or increase by ≥ 50% of previously identified site)

Time from first dosing until documentation of progression or death due to lymphoma

Time from first dosing until progression or death due to any case

Number of patients with treatment-emergent AEs rated Mild, Moderate, and Severe

Number of patients with at least one positive (+ve) post-Baseline sample containing positive anti-MOR00208 antibodies; Baseline (pre-dose) sample has to be tested negative (-ve)

The highest concentration of MOR00208 measured in serum

The time to highest concentration of MOR00208 measured in serum

The last quantifiable concentration from the first dose of MOR00208

Area under the concentration curve. The time curve from time zero (0) to the time that the last concentration above the lower limit of quantification (LLQ) is observed.

Area under the concentration curve. The time curve from time zero (0) to infinity (inf), where infinity is computed from AUC0-t + \[Ct/λZ)\]. Ct is calculated from the concentration at the last sampling time at which the sample is above LLQ.

Apparent terminal rate constant calculated from the regression analysis (slope) from the log-transformed measured concentrations on the terminal phase of the time-point concentration curve

Apparent terminal half-life calculated from ln(2)/λz

Total body clearance calculated for single or multiple doses: dose(s)/AUC(0-inf)

Apparent volume of distribution during the terminal phase, calculated from dose/(AUC(0-inf)\*λz)

Actual change from baseline will be summarized descriptively by visit for the pharmacodynamic parameter: B-cell populations

Relative change from baseline will be summarized descriptively by visit for the pharmacodynamic parameter: B-cell populations

Actual change from baseline will be summarized descriptively by visit for the pharmacodynamic parameter: T-cell populations

Relative change from baseline will be summarized descriptively by visit for the pharmacodynamic parameter: T-cell populations

Actual change from baseline will be summarized descriptively by visit for the pharmacodynamic parameter: NK cell populations

Relative change from baseline will be summarized descriptively by visit for the pharmacodynamic parameter: NK cell populations

Incidence of AEs as stratified by presence of CD19 on malignant lymphoma cells detected by tumor biopsy/aspirate during Screening

The analysis of the primary endpoint (ORR) will additionally be stratified by presence of CD19 on malignant lymphoma cells detected by tumor biopsy/aspirate during Screening

Incidence of AEs as stratified by FcγRIIa polymorphism subgroups (genotypes HH, HR, or RR)

Incidence of AEs as stratified by FcγRIIIa polymorphism subgroups (genotypes FF, FV, or VV)

The analysis of the primary endpoint (ORR) will additionally be stratified by FcγRIIa polymorphism subgroups (genotypes HH, HR, or RR)

The analysis of the primary endpoint (ORR) will additionally be stratified by FcγRIIIa polymorphism subgroups (genotypes FF, FV, or VV)

Patients were closely monitored for any kind of AE during the study. AEs were detected through physical examination, laboratory tests, or other assessments, or when volunteered by the patient in response to non-leading questioning during or between study visits. All SAEs are reported for the Safety Population, including events occurring prior to first dose of MOR00208. For non-serious AEs, only treatment-emergent events are reported (i.e., events occurring after first dose of MOR00208).

All patients received 12 mg/kg MOR00208 administered as an intravenous infusion.

Total

Patients with follicular lymphoma. All patients received 12 mg/kg MOR00208 administered as an intravenous infusion.

FL Subtype

Patients with diffuse large B-cell lymphoma. All patients received 12 mg/kg MOR00208 administered as an intravenous infusion.

DLBCL Subtype

Patients with mantle cell lymphoma. All patients received 12 mg/kg MOR00208 administered as an intravenous infusion.

MCL Subtype

Patients with other indolent non-Hodgkin's lymphoma. All patients received 12 mg/kg MOR00208 administered as an intravenous infusion.

Other iNHL

Combined group of patients with follicular lymphoma and patients with other indolent non-Hodgkin's lymphoma. All patients received 12 mg/kg MOR00208 administered as an intravenous infusion.

FL + Other iNHL

Age, Categorical

Age, Continuous

Sex: Female, Male

Asian

Black or African American

White

Other

Race/Ethnicity, Customized

Height was not collected at Screening for 2 patients (minor protocol noncompliance)

Height

Weight

Follicular lymphoma

Diffuse large B-cell lymphoma

Mantle cell lymphoma

Other indolent NHL

NHL Subtype

Per planned analyses, baseline characteristics are summarized by NHL subtype.

Medical Information

Complete remission

Partial remission

The Intent-to-treat (ITT) Population consisted of all patients who received at least one dose of study drug. Patients without any post-Baseline assessment of NHL response were included as non-responders. Per pre-specified analysis plan, efficacy analyses are summarized overall, by NHL subtype, and for the combined group comprising FL patients + other iNHL patients.

Overall Response Rate (ORR)

The ITT Population consisted of all patients who received at least one dose of study drug. Patients without any post-Baseline assessment of NHL response were included as non-responders. Per pre-specified analysis plan, efficacy analyses are summarized overall, by NHL subtype, and for the combined group comprising FL patients + other iNHL patients.

Stable Disease (SD) Rate

Patients in the ITT Population who had any response (CR or PR) during the study. Per pre-specified analysis plan, efficacy analyses are summarized overall, by NHL subtype, and for the combined group comprising FL patients + other iNHL patients.

Duration of Response (DoR)

Patients in the ITT Population with documented progression of disease. Per pre-specified analysis plan, efficacy analyses are summarized overall, by NHL subtype, and for the combined group comprising FL patients + other iNHL patients.

Time to Progression (TTP)

Patients in the ITT Population with documented progression of disease or death from any cause. Per pre-specified analysis plan, efficacy analyses are summarized overall, by NHL subtype, and for the combined group comprising FL patients + other iNHL patients.

Progression-free Survival (PFS)

Mild

Moderate

Severe

The Safety Population consisted of all patients who received at least one dose of study drug. Per pre-specified analysis plan, adverse event analyses are summarized overall, by NHL subtype, and for the combined group comprising FL patients + other iNHL patients.

Incidence and Severity of Adverse Events (AEs)

The Safety Population (all patients who received at least one dose of study drug). Per pre-specified analysis plan, statistical summaries are provided overall, by NHL subtype, and for the combined group comprising FL patients + other iNHL patients.

Number and Proportion of Patients Who Potentially Developed Anti-MOR00208 Antibodies and Semiquantitative Anti-MOR00208 Antibody Assessments

The PK Population included all patients who had at least one quantifiable serum MOR00208 concentration. PK parameters were calculated as data permitted. Per pre-specified analysis plan, statistical summaries are provided overall, by NHL subtype, and for the combined group comprising FL patients + other iNHL patients.

Pharmacokinetic (PK) Parameter: Maximum Serum Concentration Observed (Cmax) of MOR00208

PK Parameter: Time to Maximum Serum Concentration Observed (Tmax) of MOR00208

PK Parameter: Apparent Trough Serum Concentration Before Dosing (Clast) of MOR00208

PK Parameter: Area Under the Concentration Curve From Dose Time Zero to the Time the Last Quantifiable Concentration is Observed (AUC[0-t]) of MOR00208

PK Parameter: Area Under the Concentration Curve From Dose Time Zero to Infinity (AUC[0-inf]) of MOR00208

PK Parameter: Apparent Terminal Rate Constant (λz) of MOR00208

PK Parameter: Apparent Terminal Half-life (t[1/2]) of MOR00208

PK Parameter: Total Body Clearance (CL) of MOR00208

PK Parameter: Apparent Volume of Distribution (Vz) of MOR00208

Cycle 1 Day 8

Cycle 1 Day 15

Cycle 1 Day 22

Cycle 2 Day 1

Cycle 2 Day 15

Cycle 2 Day 28

Cycle 3 Day 1

Cycle 3 Day 15

Cycle 3 Day 28

Study Completion/Early Termination

Pharmacodynamic samples were collected at timepoints through the study where possible. Per pre-specified analysis plan, statistical summaries are provided overall, by NHL subtype, and for the combined group comprising FL patients + other iNHL patients.

Absolute Change From Baseline in Measurements of B-cell Populations

Percent Change From Baseline in Measurements of B-cell Populations

Absolute Change From Baseline in Measurements of T-cell Populations

Percent Change From Baseline in Measurements of T-cell Populations

Absolute Change From Baseline in Measurements of NK Cell Populations

Percent Change From Baseline in Measurements of NK Cell Populations

Per pre-specified analysis plan, if CD19 expression on tumor cells was able to be measured in less than 15% of the ITT population at screening, the stratification analyses by baseline CD19 expression (as planned in the protocol) would not be performed. It was not possible to measure CD19 expression in sufficient cases for such an analysis to be meaningful.

Evaluation of AEs Stratified by Baseline CD19 Expression on Malignant Lymphoma Cells

Evaluation of ORR Stratified by Baseline CD19 Expression on Malignant Lymphoma Cells

Genotype HH

Genotype HR

Genotype RR

Genotyping for FcγRIIa and FcγRIIIa polymorphisms was performed for patients who consented to an optional mucosal cheek swab. Per pre-specified analysis plan, statistical summaries are provided overall, by NHL subtype, and for the combined group comprising FL patients + other iNHL patients.

Evaluation of AEs Stratified by FcγRIIa Polymorphism

Genotype FF

Genotype FV

Genotype VV

Evaluation of AEs Stratified by FcγRIIIa Polymorphism

Evaluation of ORR Stratified by FcγRIIa Polymorphism

Evaluation of ORR Stratified by FcγRIIIa Polymorphism

Main Study Treatment (Cycles 1 - 2)

Cycle 3 and Maintenance Treatment

Leukemia

Precursor Cell Lymphoblastic Leukemia-Lymphoma

Leukemia, Lymphoid

Hematologic Diseases

Acute Lymphoblastic Leukemia

Lymphoblastic Lymphoma

Acute Graft Versus Host Disease

intravenous Infusion of MOR00208, Fc-optimized Anti-CD19 Antibody

MOR00208 (formerly Xmab5574)

Elias Jabbour, MD

Rebecca Klisovic, MD

Wing H. Leung, M.D., PhD

This is an open-label, multicentre study to characterize the safety and preliminary efficacy of the human anti CD19 antibody MOR00208 in adult subjects with relapsed/refractory B-cell acute lymphoblastic leukemia (B-ALL)

Study of Fc-Optimized Anti-CD19 Antibody (MOR00208) to Treat B-cell Acute Lymphoblastic Leukemia(B-ALL)

A Phase IIa, Single-arm, Open-label Study of MOR00208, a Humanized Fc-Engineered Anti-CD19 Antibody, in Patients With Relapsed/Refractory B-cell Acute Lymphoblastic Leukemia (B-ALL)

ORR= CR (Complete Remission) + PR (Partial Remission)

Antitumor activity of MOR00208

Two patients had a response to treatment. For one of the two patients a progression was recorded, the other patient was censored due to an AE. Conse quently, the planned Kaplan-Meier analyses of response duration and time to hematological relapse could not be calculated.

Number of patients with at least one treatment-emergent AE

Steady State Trough Plasma Concentration (Cpre-dose) at 9th dose (infusion)

Number of patients with treatment-emergent AEs

intravenous Infusion of MOR00208, Fc-optimized Anti-CD19 Antibody

MOR00208 (formerly Xmab5574)

Total Patients Screened: 30 Total patients Enrolled (at least one infusion with study treatment): 22

MOR00208 (Formerly Xmab5574)

intravenous Infusion of MOR00208, Fc-optimized Anti-CD19 Antibody

MOR00208 (formerly Xmab5574)

Body Mass Index

Dr. Sumeet Ambarkhane, Director, Clinical Program Leader

Responder 1

Responder 2

Patients Response Duration Evaluation by Hematology, Bone Marrow Aspirates or Biopsy, CT

Safety Will be Evaluated by Assessing Adverse Events, Clinical Lab Data and Vital Signs, ECG, Physical Exam

Pharmacokinetics of MOR00208

Anti-MOR208 antibodies were not observed in any patients treated during this study.

Study title	NCT ID	Conditions	Interventions	Eligibility	Organization
Phase Ib Study to Assess Safety and Preliminary Efficacy of Tafasitamab or Tafasitamab Plus Lenalidomide in Addition to R-CHOP in Patients With Newly Diagnosed DLBCL	NCT04134936	Diffuse Large B...	Tafasitamab Tafasitamab plu...	18 Years -	MorphoSys AG
Phase Ib Study to Assess Safety and Preliminary Efficacy of Tafasitamab or Tafasitamab Plus Lenalidomide in Addition to R-CHOP in Patients With Newly Diagnosed DLBCL	NCT04134936	Diffuse Large B...	Tafasitamab Tafasitamab plu...	18 Years -	MorphoSys AG
Study of Fc-Optimized Anti-CD19 Antibody (MOR00208) to Treat Non-Hodgkin's Lymphoma (NHL)	NCT01685008	Non-Hodgkin Lym...	MOR00208 (forme...	18 Years -	MorphoSys AG
Study of Fc-Optimized Anti-CD19 Antibody (MOR00208) to Treat B-cell Acute Lymphoblastic Leukemia(B-ALL)	NCT01685021	Acute Lymphobla...	MOR00208 (forme...	16 Years -	MorphoSys AG
Phase II MOR00208 in Combination With Lenalidomide for Patients With Relapsed or Refractory CLL, SLL or PLL or Older Patients With Untreated CLL, SLL or PLL	NCT02005289	Contiguous Stag... Noncontiguous S... Prolymphocytic ... Recurrent Small... Refractory Chro... Stage I Chronic... Stage I Small L... Stage II Chroni... Stage III Chron... Stage III Small... Stage IV Chroni... Stage IV Small ...	MOR00208 lenalidomide Correlative Stu...	18 Years - 80 Years	Ohio State University Comprehensive Cancer Center
Phase II MOR00208 in Combination With Lenalidomide for Patients With Relapsed or Refractory CLL, SLL or PLL or Older Patients With Untreated CLL, SLL or PLL	NCT02005289	Contiguous Stag... Noncontiguous S... Prolymphocytic ... Recurrent Small... Refractory Chro... Stage I Chronic... Stage I Small L... Stage II Chroni... Stage III Chron... Stage III Small... Stage IV Chroni... Stage IV Small ...	MOR00208 lenalidomide Correlative Stu...	18 Years - 80 Years	Ohio State University Comprehensive Cancer Center

Spots Global Cancer Trial Database for mor208

Every month we try and update this database with for mor208 cancer trials from around the world to help patients and their families find trials that might be right for them.
We offer this 100% free of charge and do not endorse any of the trials listed here, we hope it helps you or a loved one.

Spots Global Cancer Trial Database for mor208

Every month we try and update this database with for mor208 cancer trials from around the world to help patients and their families find trials that might be right for them. We offer this 100% free of charge and do not endorse any of the trials listed here, we hope it helps you or a loved one.

Every month we try and update this database with for mor208 cancer trials from around the world to help patients and their families find trials that might be right for them.
We offer this 100% free of charge and do not endorse any of the trials listed here, we hope it helps you or a loved one.