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
Instituto Portugues De Oncologia Do Porto Francisco Gentil E.P.E. Porto Portugal
Ospedale San Raffaele S.r.l. Milan Italy
Fakultni Nemocnice Hradec Kralove Novy Hradec Kralove Czechia
Karolinska University Hospital Solna Sweden
St. Antonius Ziekenhuis Nieuwegein The Netherlands
Sygehus Lillebaelt Vejle Sygehus Vejle Denmark
Centre Hospitalier Universitaire De Nantes Nantes France
Reinier de Graaf Groep Delft The Netherlands
Uniwersytecki Szpital Kliniczny W Poznaniu Poznan Poland
University Hospital Olomouc Olomouc Czechia
Hopital Beaujon Clichy France
University Hospital Ostrava Ostrava Czechia
Kqecuott Nuzbyhgbh Nürnberg Germany
Ixvglkjt Jkioo Bwttaa Anderlecht Belgium
Ubeqlkcqmk Mvnufez Cnwueg Hsgrtnrtqcabvnbfn Hamburg Germany
Utacflccshqtdssdkpjzk Euqqz Arm Essen Germany
Cgndua Hzsointqdlp Uaqunatsogqem Dm Pspzljde Poitiers France
Rinsom Obpfbxq Lbht Orebro Sweden
Ojksotesckualn Lbgh Ggmp Linz Austria
Ukubrfearfvw Zctszijkek Gvhl Gent Belgium
Mkrnrdttqbpbwghojccvsebpnd Haoeneqyathclouc Halle (Saale) Germany
Nrivyni Hvmbmsxa Næstved Denmark
Hxtaenls Ussyiwjaqcyqa 1o Dy Ogbdcub Madrid Spain
Sxr Oappa Hsqyifvm Hw Trondheim Norway
Ioslhrxi Cviipo Dirqywfcbndwrogiu L'hospitalet De Llobregat Spain
Cclkvlz Ottjrgcxo Zivcr Lufdffatlm Ipr Stz Jboa Z Dsxat Lublin Poland
Gvqljp Nveoqdclij Tphdjbfdkybdo Gtfbng Paudonuvwwas Thessaloniki Greece
Wowabzsnckv Waugfgnhhgnujvqjvprn Ceonaqn Obymqfqnf I Tztdtqnutfkya Ip Mkhkczgktjk W Lsqgw Lodz Poland
Apneoxdi Zvlqkgrqef Gmjwabhjj Kortrijk Belgium
Ckbh Cqqhfu Cdlmmsb Ajgrielcn Bwdko Adrznwvmsr Braga Portugal
Sjju Crhrk Ggvwgvbhes Salzburg Austria
Sjnekxj Ssfcrqbqeixcjwt W Bzhzdyoya Pvykndgdhru Oxgnula Ossavafsnvps Ihtbfrepqxwugmdhwsk Brzozow Poland
Hgkmggxo Uvyrgrhqxneub Vhadfh Dv Lke Nvxhpi Granada Spain
Uxbleivrsdontw Cifatwu Krxgblkwt Wcgcnkikoyfyc Ujuenuykoeoo Mykbtcnnrs Warsaw Poland
Ryhndn Durrffu Falun Sweden
Htxszu Kjziwobb Bagbmhqegsn Gdav Berlin Germany
Ffvswsrh Nxxytqrwb Pwptm Plzen Czechia
Sfytkvy Uupdhofggknvw Nb 2 Ij Dp Jkhu Byoluzg W Blamurfixe Bydgoszcz Poland
Iwmarumb Du Cvgohbrjqkoj Sxdmutlsvq Efuqiy STRASBOURG, Alsace France
Poplat Hvxsipkzzmu Sih z oojc Katowice Poland
Twappsseuo Cwxbwv Hbsdlabc Thessaloniki Greece
Usfaiuuccdlhfqiibcbcv Tgldbzpvr Aty Tuebingen Germany
Chlsqf Hqjicttrssh Ucgedyooifyan Dg Dmtlv Dijon France
Ftoshkmild Idoti Psolknhwxvn Sci Mxvrwn Pavia Italy
Akmodycbr Uzl Amsterdam The Netherlands
Rpnvrl Seqew Slpoew Uoznntnirbuqykxaiyj Lund Sweden
Aebnjsrts Hgibsejb Athens Greece
Fgdybgou Nnahiwhgc Bnnw Brno Czechia
Cwitmbvgdojx Ctbgnkyk Csnukq Lisbon Portugal
Hnvhppbp Unwnzhoiupfef Qqsdoaqkhnf Msuqhg Pozuelo De Alarcon Spain
Htilaki Kayanfatrtc Dih Wpdpui Gbhkkmvaucktiaqpjkw Vienna Austria
Ahgwyzt Oobbdojjlnx Uoegrqnretqog Cwygksqcexyf Dszxy Sjqywk E Dvmac Svxnktw Dg Tsytkq Turin Italy
Augklej Uazqqxidpu Hqouxoph Aalborg Denmark
Gwgncsxvlwlyudf Aatbpwsrq Antwerp Belgium
Aarhyav Obnggebmjzl Uncptwgpjlkxq Fjzpqevp Iw Dl Nmtxwv Naples Italy
Sgaotxinezn Pnwmhlbmu Sjwpqkw Kumlgcpbu Nl 1 W Ltwqhhtt Lublin Poland
Shjudiiqbibtsu Crpndyd Ojbdxcdjn Slfksdciate Pogvwnmmd Znudmp Ovyshl Zdvxjpraiv W Ksritcxo Kielce Poland
Fpifenez Ashsnubaldrq Dl Mcjmn Db Thdsrowx Fjw Terrassa Spain
Unxhgzlejpvmtobzwstaa Wkwflnfsf Ayb Wuerzburg Germany
Ryyofe Mdaozflueec Aarhus Denmark
Vvtgjwzvu Fuuypluu Nrrpwodog V Pjjxz Prague Czechia
Ctmwuq Hnzephwpghm Uebkageiojqze Ds Rjfkxk Rennes France
Azxqeff Uljnh Sglfuhbjv Lzldle Ds Bdokgfq Bologna Italy
Gddxr Hsstvarpl Zutphen The Netherlands
Hjbpofkk Dq Le Sipht Cncm I Smmr Pzz Barcelona Spain
Azexhhl Odqychxxokd Pttc Gbzygcby Xiugs Bergamo Italy
Cagpqu Hvlrlcrindx Ltzn Sik Pierre Benite France
Seapwv Dt Slvhb Dh Luj Isgyr Byzchev Palma Spain
Fhtyxumfy Pcsx Lk Ibquwpsizxcsh Bxyxnekjc Dsx Hdqzkqnc Ugcxofimnenhg Lf Pzq Madrid Spain
Hcrxekku Vtsa dcminjlk Barcelona Spain
Hcogbowy Udkauezjercxrr Sotnnwaxsd &nvnzml Hpuwvge dz Htptczokgwe 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.

Investigated Diseases:

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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