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Diffuse Large B Cell LymphomaPhase 1/2MINDwayNCT05222555

Safety and Pharmacokinetics Study of a Modified Tafasitamab IV Dosing Regimen Combined With Lenalidomide in R-R DLBCL Patients

A Phase 1/2 study testing Tafasitamab and Lenalidomide in people with Diffuse Large B Cell Lymphoma, run by Incyte Corporation at 62 sites in 9 countries.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

This is an open-label, multicentre study too Evaluate the Safety and Pharmacokinetics of a Modified Tafasitamab IV Dosing Regimen Combined with Lenalidomide (LEN) in Patients with Relapsed or Refractory Diffuse Large B-Cell Lymphoma (R/R DLBCL) who have had at least one, but no more than three prior systemic regimens… Read more about this study

Who is it for?
Ages 18 to 99 years
Conditions the study is for
Diffuse Large B Cell Lymphoma
What is being tested?
Tafasitamab and Lenalidomide
Could I receive a placebo?
No, everyone receives an active treatment
How many people
53 participants
Where
62 sitesin 9 countries
Study dates
19 Jul 2022to 30 Nov 2027
Phase
Phase 1/2
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 99 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Major Inclusion Criteria:

  1. Capable of giving signed informed consent
  2. Age 18 years or older
  3. Histologically confirmed diagnosis of DLBCL
  4. Tumor tissue for retrospective central pathology review must be provided as an adjunct to participation in this study.
  5. Patients must have:
  • relapsed and/or refractory disease
  • at least one bidimensionally measurable, PET positive disease site (transverse diameter of ≥1.5 cm and perpendicular diameter of ≥1.0 cm at baseline)
  • received at least one, but no more than three previous systemic regimens for the treatment of DLBCL and one therapy line must have included a CD20-targeted therapy
  • Eastern Cooperative Oncology Group 0 to 2
  1. Patients not considered in the opinion of the investigator eligible to undergo intensive salvage therapy including ASCT
  2. Patients must meet the following laboratory criteria at screening:
  • absolute neutrophil count ≥1.5 × 10^9/L
  • platelet count ≥90 × 10^9/L
  • total serum bilirubin ≤2.5 × ULN or ≤5 × ULN in cases of Glibert's Syndrome or liver involvement by lymphoma
  • alanine transaminase, aspartate aminotransferase and alkaline phosphatase ≤3 × ULN or <5 × ULN in cases of liver involvement
  • serum creatinine clearance ≥ 60 mL/minute
  1. Patients who received previous CD19 targeted therapy (other than tafasitamab) must have CD19 positive lymphoma confirmed on a biopsy taken since completing the prior CD19 targeted therapy
  2. Patients with primary refractory disease who received at least one, but no more than three previous systemic regimens (including a CD20 targeted therapy)

Major Exclusion Criteria:

  1. Patients who are legally institutionalized or concurrent enrollment in another interventional clinical study
  2. Patients who have:
  • other histological type of lymphoma
  • a history of "double/triple hit" genetics
  1. Patients who have, within 14 days prior to Day 1 dosing:
  • not discontinued CD20-targeted therapy, chemotherapy, radiotherapy, investigational anticancer therapy or other lymphoma specific therapy
  • undergone major surgery (with 4 weeks) or suffered from significant traumatic injury
  • received live vaccines (within 4 weeks).
  • required parenteral antimicrobial therapy for active, intercurrent infections
  1. Patients who:
  • have not recovered sufficiently from the adverse toxic effects of prior therapies
  • were previously treated with IMiDs® (e.g. thalidomide, LEN)
  • have history of hyper sensitivity to compounds of similar biological or chemical composition to tafasitamab IMiDs® and/or the excipients contained in the study treatment formulations
  • have undergone ASCT within the period ≤ 3 months prior to signing the informed consent form.
  • have undergone previous allogenic stem cell transplantation
  • have a history of deep venous thrombosis/embolism and who are not willing/able to take venous thromboembolic event prophylaxis during the entire treatment period
  • concurrently use other anticancer or experimental treatments
  1. History of other malignancy that could affect compliance with the protocol or interpretation of results. Exceptions
  • Patients with any malignancy appropriately treated with curative intent and the malignancy has been in remission without treatment for >2 years prior to enrollment are eligible
  • Patients with low-grade, early-stage prostate cancer (Gleason score 6 or below, Stage 1 or 2) with no requirement for therapy at any time prior to study are eligible
  1. Patients with:
  • positive hepatitis B and/or C serology.
  • known seropositivity for or history of active viral infection with human immunodeficiency virus (HIV)
  • CNS lymphoma involvement
  • history or evidence of clinically significant cardiovascular, CNS and/or other systemic disease that would in the investigator's opinion preclude participation in the study or compromise the patient's ability to give informed consent
  • history or evidence of rare hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption
  • gastrointestinal (GI) abnormalities (issue with absorption) including the inability to take oral medication
  • history or evidence of severe hepatic impairment (total serum bilirubin > 3mg/dL), jaundice unless secondary to Gilbert's syndrome or documented liver involvement by lymphoma
  • history of hypersensitivity to any of the study treatments or its excipients or to drugs of similar chemical class
  • any other medical condition which, in the investigator's opinion, makes the patient unsuitable for the study
  1. Female participants: Agreement to remain abstinent (refrain from heterosexual intercourse) or use contraceptive methods and refrain from breast feeding and donating eggs; agreement to ongoing pregnancy testing during the course of the study, and after study therapy has ended Male participants: agreement to remain abstinent (refrain from heterosexual intercourse) or use a condom and agreement to refrain from donating sperm

Trial locations and contacts

62 sites in 9 countries.

62 sites in 9 countries

South Korea12 sites
  • Dong-A University Medical Center

    Busan, 49201

  • Pusan National University Hospital

    Busan, 49241

  • Kosin University Gospel Hospital

    Busan, 49267

  • Yeungnam University Hospital

    Daegu, 42415

  • Daegu Catholic University Medical Center

    Daegu, 42472

  • Gachon University Gil Medical Center

    Incheon, 21565

  • Chonbuk National University Hospital

    Jeonju, 54907

  • Hanyang University Medical Center

    Seoul, 4763

  • Asan Medical Center - PPDS

    Seoul, 5505

  • The Catholic University of Korea, Yeouido St. Mary's Hospital

    Seoul, 7345

  • The Catholic University of Korea, St. Vincent's Hospital

    Suwon, Gyeonggido, 16247

  • Ulsan University Hospital

    Ulsan, 44033

Other trials in South Korea

Poland11 sites
  • Szpitale Pomorskie Sp. z o. o.

    Gdynia, 81-519

  • Pratia MCM Krakow

    Krakow, Lesser Poland Voivodeship, 30-510

  • SP ZOZ Szpital Uniwersytecki w Krakowie

    Krakow, 31-501

  • Wojewodzkie Wielospecjalistyczne Centrum Onkologii i Traumatologii im. M. Kopernika w Lodzi

    Lodz, 93-513

  • SPZOZ MiSWiA z Warminsko-Mazurskim Centrum Onkologii w Olsztynie

    Olsztyn, 10-228

  • Szpital Wojewodzki w Opolu

    Opole, Opole Voivodeship, 45-061

  • Centrum Medyczne Poznan - PRATIA - PPDS

    Skórzewo, Greater Poland Voivodeship, 60-185

  • Nasz Lekarz Osrodek Badan Klinicznych

    Torun, 87-100

  • Narodowy Instytut Onkologii im. Marii Sklodowskiej-Curie - Panstwowy Instytut Badawczy

    Warsaw, Masovian Voivodeship, 02-781

  • Uniwersytecki Szpital Kliniczny im. Jana Mikulicza Radeckiego we Wroclawiu

    Wroclaw, Lower Silesian Voivodeship, 50-367

  • Dolnoslaskie Centrum Onkologii, Pulmonologii i Hematologii

    Wroclaw, Lower Silesian Voivodeship, 53-439

Other trials in Poland

Spain11 sites
  • Institut Catala d'Oncologia Girona

    Girona, 17007

  • ICO l'Hospitalet - Hospital Duran i Reynals

    L'Hospitalet de Llobregat, 8907

  • Hospital U. Infanta Leonor

    Madrid, 28031

  • MD Anderson Madrid

    Madrid, 28033

  • Hospital U. Ramon y Cajal

    Madrid, 28034

  • Hospital Universitario Fundacion Jimenez Diaz

    Madrid, 28040

  • Hospital U. Quironsalud Madrid

    Madrid, 28223

  • Hospital Son Llatzer

    Palma de Mallorca, Balearic Islands, 7198

  • Complejo Asistencial Universitario de Salamanca - H. Clinico

    Salamanca, 37007

  • Hospital U. Virgen del Rocio

    Seville, 41013

  • Hospital Universitari La Fe

    Valencia, 46026

Other trials in Spain

Italy8 sites
  • Fondazione del Piemonte per l'Oncologia (IRCCS)

    Candiolo, Piedmont, 10060

  • Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico

    Milan, Lombardy, 20122

  • ASST Grande Ospedale Metropolitano Niguarda - Presidio Ospedaliero Ospedale Niguarda

    Milan, Lombardy, 20162

  • ASST di Monza - Azienda Ospedaliera San Gerardo

    Monza, Monza E Brianza, 20900

  • Fondazione IRCCS Policlinico San Matteo di Pavia

    Pavia, Lombardy, 27100

  • Azienda Ospedaliera di Perugia

    Perugia, Umbria, 6122

  • Azienda Ospedaliero Universitaria Pisana

    Pisa, Tuscany, 56127

  • Ospedale Santa Maria Delle Croci

    Ravenna, Emilia-Romagna, 48121

Other trials in Italy

Czechia5 sites
  • Fakultni nemocnice Brno

    Brno, 625 00

  • Fakultni nemocnice Ostrava

    Ostrava, 708 52

  • Fakultni nemocnice Kralovske Vinohrady

    Prague, 100 34

  • Vseobecna Fakultni Nemocnice V Praze

    Prague, 128 08

  • Fakultni nemocnice v Motole

    Prague, 150 06

Other trials in Czechia

Israel5 sites
  • Shamir Medical Center Assaf Harofeh

    Be’er Ya‘aqov, 70300

  • Soroka University Medical Centre

    Beersheba, Southern District, 84101

  • Lady Davis Carmel Medical Center

    Haifa, 34362

  • Hadassah Medical Center - Hadassah Ein Kerem

    Jerusalem, 91120

  • ZIV Medical Center

    Safed, 13100

Other trials in Israel

France4 sites
  • Centre Hospitalier Universitaire Grenoble Alpes - Hopital Albert Michallon

    Grenoble, Isère, 38043

  • Centre Hospitalier Le Mans

    Le Mans, Sarthe, 72000

  • CHU Nantes

    Nantes, Loire-Atlantique, 44000

  • CHU de Poitiers

    Poitiers, Vienne, 86021

Other trials in France

United States3 sites
  • Texas Oncology-Baylor Charles A. Sammons Cancer Center - USOR

    Dallas, Texas, 75246-2092

  • Morristown Memorial Hospital

    Morristown, New Jersey, 07960-6459

  • Vista Oncology

    Olympia, Washington, 98506

Other trials in United States

Austria3 sites
  • Universitatsklinikum Salzburg

    Salzburg, 5020

  • UK St. Pölten

    Sankt Pölten, Lower Austria, 3100

  • Klinikum Wels Grieskirchen

    Wels, Upper Austria, 4600

Other trials in Austria

About this study

Official title: A Phase 1b/2, Open-Label, Multicenter Study to Evaluate the Safety and Pharmacokinetics of a Modified Tafasitamab IV Dosing Regimen Combined With Lenalidomide in Patients With Relapsed or Refractory Diffuse Large B-Cell Lymphoma

This is an open-label, multicentre study too Evaluate the Safety and Pharmacokinetics of a Modified Tafasitamab IV Dosing Regimen Combined with Lenalidomide (LEN) in Patients with Relapsed or Refractory Diffuse Large B-Cell Lymphoma (R/R DLBCL) who have had at least one, but no more than three prior systemic regimens and who are not eligible for high dose chemotherapy (HDC) with autologous stem-cell transplantation (ASCT) at the time of study entry.

Being tested
Tafasitamab, Lenalidomide
Keywords
monoclonal antibody, CD19, tafasitamab
Medical subject headings
Lymphoma, Large B-Cell, Diffuse

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • TafasitamabDrug

    Also called INCMOR00208, MOR00208, Xmab5574

    tafasitamab will be administered intravenously at protocol defined timepoints

  • LenalidomideDrug

    lenalidomide will be administered orally at protocol defined timepoints

Study groups in NCT05222555
Study groupRoleWhat they receive
Treatment (Tafasitamab + Lenalidomide)ExperimentalTreatment: Tafasitamab will be combined with lenalidomide in R/R DLBCL patients. Dose: Cohort 1: The dose of tafasitamab will be level 1 high dose in combination with the approved dose Cohort 2: The dose of tafasitamab will be level 2 high dose in combination with the approved dose Expansion Cohort: The dose of tafasitamab will be the dose that is deemed safe and tolerable as determined from cohort 1 \& cohort 2 Treatment consisting of tafasitamab and lenalidomide combination will be administered until disease progression, unacceptable toxicity, or discontinuation for any other reason, whichever comes first. Lenalidomide can be given for up to 12 cycles in total, after which patients can continue with tafasitamab as monotherapy until progression or unacceptable toxicity.
Receives: Drug: Tafasitamab; Drug: Lenalidomide

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of Participants With Any Treatment-emergent Adverse Event (TEAE)

    An adverse event (AE) was defined as any untoward medical occurrence in a participant temporally associated with the use of study treatment, whether or not considered related to the study treatment. Therefore, an AE could be any unfavorable or unintended sign (including an abnormal laboratory finding) or symptom temporally associated with the use of study treatment. A TEAE was defined as any AE that started or worsened after the first dose of study treatment until 90 days after the last dose of the study treatment. An AE that was present prior to study drug administration but increased in severity after treatment start was also included as a TEAE.

    Measured: up to approximately 2 years

  2. Number of Participants With Any ≥Grade 3 TEAE

    The toxicity grade of TEAEs was graded using the National Cancer Institute-Common Terminology Criteria for Adverse Events version 5.0 (NCI-CTCAE v5.0) using the following definitions: Grade 1: mild; asymptomatic or mild symptoms; clinical or diagnostic observations only; intervention not indicated. Grade 2: moderate; minimal; local or non-invasive intervention indicated; limiting age-appropriate instrumental activities of daily living (refers to preparing meals, shopping for groceries or clothes, using the telephone, managing money, etc.). Grade 3: severe or medically significant but not immediately life threatening; hospitalization or prolongation of hospitalization indicated; disabling; limiting self-care activities of daily living. Grade 4: life-threatening consequences; urgent intervention indicated. Grade 5: death related to AE.

    Measured: up to approximately 2 years

Secondary outcomes (6)
  1. Ctrough of Tafasitamab After 3 and 12 Treatment Cycles

    Ctrough was defined as the minimum concentration of tafasitamab.

    Measured: predose on Cycle 3 Day 15; predose on Cycle 12 Day 28 (up to approximately 1 year [after twelve 28-day cycles])

  2. Cmax of Tafasitamab After 3 Treatment Cycles

    Cmax was defined as the maximum observed plasma concentration of tafasitamab.

    Measured: 30 minutes after the end of tafasitamab infusion on Cycle 3 Day 15 (up to approximately 85 days [after three 28-day cycles])

  3. Best Objective Response Rate (ORR) by Investigator Assessment up to Treatment Cycle 12

    ORR was defined as the percentage of participants with complete response (CR: disappearance of all evidence disease) or partial response (PR: regression of measurable disease and no new sites) as the best response achieved at any time during the study. Only responses of CR or PR that were documented before the initiation of new antilymphoma therapy (NALT) were considered. Response assessments were based on revised International Working Group response criteria for malignant lymphoma.

    Measured: up to 19.8 months

  4. Duration of Response (DoR) by Investigator Assessment

    Measured: up to approximately 64 months (approximately 5 years)

  5. Progression-free Survival (PFS) by Investigator Assessment

    Measured: up to approximately 64 months (approximately 5 years)

  6. Number of Participants Developing Anti-tafasitamab Antibodies up to Treatment Cycle 12

    Anti-tafasitamab antibody samples were defined as negative if they were screened or confirmed negative. Anti-tafasitamab antibody samples were defined as positive if they were positive in both the screening and the confirmatory assays.

    Measured: up to approximately 1 year (after twelve 28-day cycles)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Feb 2022
  2. Study start19 Jul 2022
  3. Primary completion17 Jul 2024
  4. Study completion30 Nov 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1/2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
53 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05222555
Sponsor's protocol ID
MOR208C115
Other IDs
2023-507993-42-00, 2021-003855-40, 2023
Acronym
MINDway
Status last verified
Jan 2026
First submitted
11 Jan 2022
Last updated
16 Jan 2026
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 1/2 study testing Tafasitamab and Lenalidomide in people with Diffuse Large B Cell Lymphoma, run by Incyte Corporation at 62 sites in 9 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 16 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 62 sites in South Korea, Poland, Spain, Italy, Czechia and 4 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this combined phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 28 Jul 2025). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of Participants With Any Treatment-emergent Adverse Event (TEAE) (time frame: up to approximately 2 years). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Jan 2026.

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