Study Comparing Teclistamab, Talquetamab, and Drug Combination for Patients with Newly Diagnosed Multiple Myeloma Not Suitable for Stem Cell Transplant

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What is this study about?

This clinical trial is focused on studying treatments for Multiple Myeloma, a type of blood cancer that affects plasma cells in the bone marrow. The study will compare different combinations of medications to see which is more effective. The medications being tested include Teclistamab and Talquetamab, both used in combination with Daratumumab and Lenalidomide. Another group will receive a combination of Daratumumab, Lenalidomide, and Dexamethasone. These medications are given as injections or capsules.

The purpose of the study is to compare the effectiveness of these different treatment combinations in people who have been newly diagnosed with Multiple Myeloma and are not eligible for a stem cell transplant as their initial therapy. Participants will be randomly assigned to one of the treatment groups and will receive their assigned treatment over a period of time. The study will monitor the participants’ health and response to the treatment to determine which combination works best.

Throughout the study, participants will receive regular check-ups and monitoring to ensure their safety and to track the progress of the treatment. The study aims to provide valuable information on the best treatment options for people with Multiple Myeloma who cannot undergo a stem cell transplant.

1 initial treatment phase

Upon joining the study, the patient will begin the initial treatment phase. This phase involves the administration of medications designed to treat multiple myeloma, a type of blood cancer.

The patient will receive a combination of medications, which may include teclistamab, talquetamab, daratumumab, lenalidomide, and dexamethasone. These medications are administered in different forms such as injections and oral capsules or tablets.

2 medication administration

The patient will receive teclistamab and talquetamab as a solution for injection, administered subcutaneously, which means under the skin.

The patient will also take lenalidomide in the form of hard capsules, and dexamethasone in tablet form, both taken orally.

3 treatment regimen

The treatment regimen involves a combination of these medications, with specific dosages and frequencies determined by the study protocol. The exact schedule will be provided by the healthcare team overseeing the trial.

The patient will continue this regimen for the duration specified by the study, which aims to evaluate the effectiveness of the treatment combinations.

4 monitoring and assessment

Throughout the trial, the patient’s health and response to the treatment will be closely monitored. This includes regular check-ups and assessments to track progress and any side effects.

The primary goal is to compare the effectiveness of different treatment combinations in managing multiple myeloma.

5 completion of trial

The trial is expected to continue until June 28, 2033. Upon completion, the patient’s overall response to the treatment will be evaluated.

The results will contribute to understanding the best treatment options for individuals with newly diagnosed multiple myeloma who are not candidates for stem cell transplant.

Who Can Join the Study?

  • Have a diagnosis of multiple myeloma, which is a type of blood cancer, according to specific medical guidelines.
  • Be newly diagnosed and not suitable for high-dose chemotherapy with autologous stem cell transplant (ASCT) because of:
    • Advanced age making it unsafe.
    • Other health conditions that could make the treatment difficult to handle.
    • Choosing to delay this type of treatment as the first option.
  • Have an Eastern Cooperative Oncology Group (ECOG) performance status score of 0 to 2, which is a way to measure how well you can perform daily activities.
  • Agree not to be pregnant, breastfeeding, or planning to become pregnant while in the study or for 6 months after the last treatment dose.
  • Agree not to plan to father a child while in the study or for 100 days after the last treatment dose.

Who Cannot Join the Study?

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Other Sites

Site Name City Country Status
Klinikum Nuernberg Nürnberg Germany
Institut Jules Bordet Anderlecht Belgium
Centre Hospitalier Universitaire De Poitiers Poitiers France
Region Oerebro Laen Orebro Sweden
Universitair Ziekenhuis Gent Gent Belgium
Næstved Hospital Næstved Denmark
Hospital Universitario 12 De Octubre Madrid Spain
St. Olavs Hospital HF Trondheim Norway
Centrum Onkologii Ziemi Lubelskiej Im. Sw. Jana Z Dukli Lublin Poland
Instituto Portugues De Oncologia Do Porto Francisco Gentil E.P.E. Porto Portugal
Geniko Nosokomeio Thessalonikis George Papanikolaou Thessaloniki Greece
Algemeen Ziekenhuis Groeninge Kortrijk Belgium
CCAB Centro Clinico Academico Braga Associacao Braga Portugal
SCRI CCCIT Ges.m.b.H. Salzburg Austria
Szpital Specjalistyczny W Brzozowie Podkarpacki Osrodek Onkologiczny Im.Ks.B.Markiewicza Brzozow Poland
Hospital Universitario Virgen De Las Nieves Granada Spain
Uniwersyteckie Centrum Kliniczne Warszawskiego Uniwersytetu Medycznego Warsaw Poland
Region Dalarna Falun Sweden
HELIOS Klinikum Berlin-Buch GmbH Berlin Germany
Fakultni Nemocnice Plzen Plzen Czechia
Szpital Uniwersytecki Nr 2 Im Dr Jana Biziela W Bydgoszczy Bydgoszcz Poland
Institut De Cancerologie Strasbourg Europe STRASBOURG, Alsace France
Pratia Hematologia Sp. z o.o. Katowice Poland
Universitaetsklinikum Tuebingen AöR Tuebingen Germany
Ospedale San Raffaele S.r.l. Milan Italy
Fondazione IRCCS Policlinico San Matteo Pavia Italy
Region Skane Skanes Universitetssjukhus Lund Sweden
Alexandra Hospital Athens Greece
Fakultni Nemocnice Brno Brno Czechia
Fakultni Nemocnice Hradec Kralove Novy Hradec Kralove Czechia
Karolinska University Hospital Solna Sweden
St. Antonius Ziekenhuis Nieuwegein The Netherlands
Champalimaud Clinical Centre Lisbon Portugal
Hospital Universitario Quironsalud Madrid Pozuelo De Alarcon Spain
Hanusch Krankenhaus Der Wiener Gebietskrankenkasse Vienna Austria
Sygehus Lillebaelt Vejle Sygehus Vejle Denmark
Aalborg University Hospital Aalborg Denmark
Gasthuiszusters Antwerpen Antwerp Belgium
Centre Hospitalier Universitaire De Nantes Nantes France
Reinier de Graaf Groep Delft The Netherlands
Samodzielny Publiczny Szpital Kliniczny Nr 1 W Lublinie Lublin Poland
Swietokrzyskie Centrum Onkologii Samodzielny Publiczny Zaklad Opieki Zdrowotnej W Kielcach Kielce Poland
Fundacio Assistencial De Mutua De Terrassa Fpc Terrassa Spain
Region Midtjylland Aarhus Denmark
Vseobecna Fakultni Nemocnice V Praze Prague Czechia
Uniwersytecki Szpital Kliniczny W Poznaniu Poznan Poland
Centre Hospitalier Universitaire De Rennes Rennes France
University Hospital Olomouc Olomouc Czechia
Gelre Hospitals Zutphen The Netherlands
Centre Hospitalier Lyon Sud Pierre Benite France
Hopital Beaujon Clichy France
Servei De Salut De Les Illes Balears Palma Spain
University Hospital Ostrava Ostrava Czechia
Uybfpwviux Mibtzvj Cgzcrk Hyhqwumrgrikotnen Hamburg Germany
Uoyusqhowiqxpowpugtvq Eoyxn Api Essen Germany
Ohryrqqiuwclmu Lrwe Guej Linz Austria
Mzamndibrxkakyjttobfigpaod Hgkxglcnmtpbpien Halle (Saale) Germany
Ibrwhdas Cutsqm Dbjfwbrpvwiuqkqpp L'hospitalet De Llobregat Spain
Wobjjozdhkt Wnetznmmzunrzvoedvjl Cyeyuen Ouvrwslfu I Tvqjzthnhnsnu Ii Mphvnlpuafi W Lyhzn Lodz Poland
Tqbczlbdul Cgucvj Hekdatsn Thessaloniki Greece
Cttqdn Hucfvqwfvjf Umouwuhlbiwmr De Dvtui Dijon France
Ahrvpmxlk Uwf Amsterdam The Netherlands
Ahtojap Owmxzzvabto Uxxjutptoeagu Czcnfagbqoxb Daxyq Scnaya E Dhqoq Sjqrajh Di Txhcbw Turin Italy
Utfvezqiprrtcfzuechvo Wvpufuxau Aas Wuerzburg Germany
Akgtmxn Uppsx Sovxstohc Lajtqz Dr Byxhhtz Bologna Italy
Hqdpgwya Dk Ll Shiaz Cpov I Splo Paa Barcelona Spain
Apjalrs Okxsnpamheb Piij Gcuyyzhk Xnojh Bergamo Italy
Fgwdoowuu Pnmj Lj Ietylfsquourj Bnuesmdsb Doz Hrvvgvna Umyxszdscjluk Lc Pyk Madrid Spain
Hzjvaavc Vwzg dzkpfztp Barcelona Spain
Hcfugfpe Uenmlutljhanxa Slfevcpuad &yqojrm Hqlocpl dh Helcivtacfa STRASBOURG, Alsace France

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Austria Austria
Not recruiting
28.09.2022
Belgium Belgium
Not recruiting
28.09.2022
Czechia Czechia
Not recruiting
28.09.2022
Denmark Denmark
Not recruiting
28.09.2022
France France
Not recruiting
28.09.2022
Germany Germany
Not recruiting
28.09.2022
Greece Greece
Not recruiting
28.09.2022
Italy Italy
Not recruiting
28.09.2022
Norway Norway
Not recruiting
28.09.2022
Poland Poland
Not recruiting
28.09.2022
Portugal Portugal
Not recruiting
28.09.2022
Spain Spain
Not recruiting
28.09.2022
Sweden Sweden
Not recruiting
28.09.2022
The Netherlands The Netherlands
Not recruiting
28.09.2022

Trial locations

Teclistamab is an investigational medication being studied for its potential to treat multiple myeloma. It is used in combination with other medications to see if it can help control the disease more effectively.

Daratumumab SC is a medication used to treat multiple myeloma. It is given as a subcutaneous injection, which means it is injected under the skin. It works by helping the immune system to attack and destroy cancer cells.

Lenalidomide is a medication that helps to slow down or stop the growth of cancer cells. It is often used in combination with other treatments for multiple myeloma to improve their effectiveness.

Talquetamab is another investigational medication being tested for its ability to treat multiple myeloma. It is used in combination with other drugs to determine if it can provide better outcomes for patients.

Dexamethasone is a type of steroid medication that helps reduce inflammation and suppress the immune system. In the context of multiple myeloma, it is used to help control symptoms and enhance the effects of other cancer treatments.

Multiple Myeloma – Multiple Myeloma is a type of blood cancer that affects plasma cells, which are a kind of white blood cell found in the bone marrow. In this disease, cancerous plasma cells multiply and accumulate in the bone marrow, leading to bone damage and affecting the production of normal blood cells. As the disease progresses, it can cause symptoms such as bone pain, frequent infections, anemia, and kidney problems. The abnormal plasma cells produce a large amount of a single type of antibody, which can be detected in the blood or urine. Over time, the accumulation of these cells and proteins can lead to complications affecting various organs and systems in the body.

Trial ID:
2023-503442-30-00
Protocol code:
64007957MMY3005
Trial Phase:
Therapeutic confirmatory (Phase III)

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