Phase 3 Study of Teclistamab in Combination With Lenalidomide and Teclistamab Alone Versus Lenalidomide Alone in Participants With Newly Diagnosed Multiple Myeloma as Maintenance Therapy Following Autologous Stem Cell Transplantation

Study Purpose

This is a multicenter, randomized, open-label, Phase 3 study in participants with newly diagnosed multiple myeloma to evaluate the benefits of teclistamab in combination with lenalidomide and teclistamab alone versus lenalidomide alone as maintenance therapy after autologous stem cell transplant.

Recruitment Criteria

Accepts Healthy Volunteers

Healthy volunteers are participants who do not have a disease or condition, or related conditions or symptoms

No
Study Type

An interventional clinical study is where participants are assigned to receive one or more interventions (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.


An observational clinical study is where participants identified as belonging to study groups are assessed for biomedical or health outcomes.


Searching Both is inclusive of interventional and observational studies.

Interventional
Eligible Ages 18 Years and Over
Gender All
More Inclusion & Exclusion Criteria

Inclusion Criteria:

  • - Must have a new diagnosis of multiple myeloma according to IMWG criteria and have received induction +/- consolidation.
  • - Must have received only one line of therapy and achieved at least a partial response (≥PR) as per IMWG 2016 response criteria (Kumar 2016) without evidence of progression at the time of first treatment dose.
  • - Must not be intolerant to the starting dose of lenalidomide.
  • - Must not have received any maintenance therapy.
  • - Have an ECOG performance status score of 0, 1, or 2 at screening and immediately prior to the start of administration of study treatment.
  • - Have clinical laboratory values within prespecified range.

Exclusion Criteria:

  • - Received any prior BCMA-directed therapy.
  • - Any previous therapy with an immune cell redirecting agent or gene modified adoptive cell therapy (eg, chimeric antigen receptor modified T cells, NK cells).
  • - Discontinued treatment due to any AE related to lenalidomide as determined by the investigator.
  • - Progressed on multiple myeloma therapy at any time prior to screening.
  • - Received a cumulative dose of corticosteroids equivalent to ≥140 mg of prednisone within the 14 days prior to first treatment dose.
  • - Received a live, attenuated vaccine within 4 weeks before first treatment dose.
Non-live vaccines or non-replicating authorized for emergency use (eg. COVID-19) are allowed.

Trial Details

Trial ID:

This trial id was obtained from ClinicalTrials.gov, a service of the U.S. National Institutes of Health, providing information on publicly and privately supported clinical studies of human participants with locations in all 50 States and in 196 countries.

NCT05243797
Phase

Phase 1: Studies that emphasize safety and how the drug is metabolized and excreted in humans.

Phase 2: Studies that gather preliminary data on effectiveness (whether the drug works in people who have a certain disease or condition) and additional safety data.

Phase 3: Studies that gather more information about safety and effectiveness by studying different populations and different dosages and by using the drug in combination with other drugs.

Phase 4: Studies occurring after FDA has approved a drug for marketing, efficacy, or optimal use.

Phase 3
Lead Sponsor

The sponsor is the organization or person who oversees the clinical study and is responsible for analyzing the study data.

Stichting European Myeloma Network
Principal Investigator

The person who is responsible for the scientific and technical direction of the entire clinical study.

N/A
Principal Investigator Affiliation N/A
Agency Class

Category of organization(s) involved as sponsor (and collaborator) supporting the trial.

Other, Industry
Overall Status Recruiting
Countries Australia, Austria, Belgium, Brazil, Czechia, Denmark, Germany, Greece, Italy, Netherlands, Norway, Serbia, Switzerland, Turkey, United Kingdom
Conditions

The disease, disorder, syndrome, illness, or injury that is being studied.

Multiple Myeloma
Arms & Interventions

Arms

Experimental: Arm A: Teclistamab-Lenalidomide (Tec-Len)

Teclistamab will be administered via a subcutaneous injection (SC)

Active Comparator: Arm B Lenalidomide Alone (Len)

Lenalidomide orally.

Experimental: Arm C Teclistamab-Alone (Tec)

Teclistamab will be administered via a subcutaneous injection (SC)

Interventions

Drug: - Teclistamab

Teclistamab will be administered via a subcutaneous injection (SC)

Drug: - Lenalidomide

Lenalidomide will be administered orally

Contact a Trial Team

If you are interested in learning more about this trial, find the trial site nearest to your location and contact the site coordinator via email or phone. We also strongly recommend that you consult with your healthcare provider about the trials that may interest you and refer to our terms of service below.

International Sites

Flinders Medical Centre, Adelaide, Australia

Status

Not yet recruiting

Address

Flinders Medical Centre

Adelaide, ,

Site Contact

Coghlan

sarah.lonergan@emn.life

+31 107033123

Barwon Health, Geelong, Australia

Status

Recruiting

Address

Barwon Health

Geelong, ,

Site Contact

Sirdesai

sarah.lonergan@emn.life

+31 107033123

Alfred Hospital, Melbourne, Australia

Status

Recruiting

Address

Alfred Hospital

Melbourne, ,

Site Contact

Spencer

sarah.lonergan@emn.life

+31 107033123

Calvary Mater Hospital, Newcastle, Australia

Status

Recruiting

Address

Calvary Mater Hospital

Newcastle, ,

Site Contact

Janowski

sarah.lonergan@emn.life

+31 107033123

Concord Hospital, Sydney, Australia

Status

Recruiting

Address

Concord Hospital

Sydney, ,

Site Contact

Wong Doo

sarah.lonergan@emn.life

+31 107033123

St Vincent's hospital, Sydney, Australia

Status

Recruiting

Address

St Vincent's hospital

Sydney, ,

Site Contact

McCaughan

sarah.lonergan@emn.life

+31 107033123

Townsville Hospital, Townsville, Australia

Status

Recruiting

Address

Townsville Hospital

Townsville, ,

Site Contact

Choong Lai

sarah.lonergan@emn.life

+31 107033123

Clinic Ottakring, Vienna, Austria

Status

Not yet recruiting

Address

Clinic Ottakring

Vienna, ,

Site Contact

Schreder

sarah.lonergan@emn.life

+31 107033123

University Hospital Leuven, Leuven, Belgium

Status

Not yet recruiting

Address

University Hospital Leuven

Leuven, ,

Site Contact

Delforge

sarah.lonergan@emn.life

+31 107033123

AC Camargo Cancer Center, São Paulo, Brazil

Status

Not yet recruiting

Address

AC Camargo Cancer Center

São Paulo, ,

Site Contact

Lemos Moura

sarah.lonergan@emn.life

+31 107033123

University Hospital, Brno, Brno, Czechia

Status

Recruiting

Address

University Hospital, Brno

Brno, ,

University Hospital Hradec Králové, Hradec Králové, Czechia

Status

Recruiting

Address

University Hospital Hradec Králové

Hradec Králové, ,

Site Contact

Radocha

sarah.lonergan@emn.life

+31 107033123

University Hospital, Olomouc, Olomouc, Czechia

Status

Recruiting

Address

University Hospital, Olomouc

Olomouc, ,

Site Contact

Minarik

sarah.lonergan@emn.life

+31 107033123

University Hospital Ostrava, Ostrava, Czechia

Status

Recruiting

Address

University Hospital Ostrava

Ostrava, ,

University Hospital Pilsen, Pilsen, Czechia

Status

Recruiting

Address

University Hospital Pilsen

Pilsen, ,

Site Contact

Lungova

sarah.lonergan@emn.life

+31 107033123

General University Hospital, Prague, Praha, Czechia

Status

Recruiting

Address

General University Hospital, Prague

Praha, ,

Rigshospitalet, Copenhagen, Denmark

Status

Not yet recruiting

Address

Rigshospitalet

Copenhagen, ,

University Hospital of Würzburg, Würzburg, Germany

Status

Not yet recruiting

Address

University Hospital of Würzburg

Würzburg, ,

Site Contact

Einsele

sarah.lonergan@emn.life

+31 107033123

Regional General Hospital Alexandra, Athens, Greece

Status

Recruiting

Address

Regional General Hospital Alexandra

Athens, ,

St Savvas Cancer Hospital, Athens, Greece

Status

Recruiting

Address

St Savvas Cancer Hospital

Athens, ,

Bologna, Italy

Status

Recruiting

Address

A.O.U. di Bologna - Policlinico S. Orsola Malpighi

Bologna, ,

Site Contact

Zamagni

sarah.lonergan@emn.life

+31 107033123

A.O.Spedali Civili di Brescia, Brescia, Italy

Status

Recruiting

Address

A.O.Spedali Civili di Brescia

Brescia, ,

Site Contact

Belotti

sarah.lonergan@emn.life

+31 107033123

Amsterdam Medical Center, Amsterdam, Netherlands

Status

Not yet recruiting

Address

Amsterdam Medical Center

Amsterdam, ,

Site Contact

van der Donk

sarah.lonergan@emn.life

+31 107033123

Erasmus MC, Rotterdam, Rotterdam, Netherlands

Status

Not yet recruiting

Address

Erasmus MC, Rotterdam

Rotterdam, ,

Oslo University Hospital, Oslo, Norway

Status

Not yet recruiting

Address

Oslo University Hospital

Oslo, ,

Site Contact

Schjesvold

sarah.lonergan@emn.life

+31 107033123

University Clinical Center of Serbia, Belgrade, Serbia

Status

Not yet recruiting

Address

University Clinical Center of Serbia

Belgrade, ,

Kantonsspital St. Gallen, Saint Gallen, Switzerland

Status

Recruiting

Address

Kantonsspital St. Gallen

Saint Gallen, ,

Ankara University, Ankara, Turkey

Status

Not yet recruiting

Address

Ankara University

Ankara, ,

St James's University Hospital, Leeds, United Kingdom

Status

Not yet recruiting

Address

St James's University Hospital

Leeds, ,