Evidence map›Paper›PMID 42098480›Full record

ArticleTherapeutic innovation & regulatory science2026

Therapeutic Horizon in Multiple Myeloma: Analysis of the Emerging Landscape of Clinical Trials.

Marina Alacoque Rodrigues, Cristiane Aparecida Menezes de Pádua, Paula Lana de Miranda Drummond, Jéssica Soares Malta, Adriano Max Moreira Reis

Abstract read
In one paragraph

Article in Therapeutic innovation & regulatory science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Marina Alacoque RodriguesCollege of Pharmacy, Universidade Federal de Minas Gerais, 6627 Antonio Carlos Ave, Belo Horizonte, Minas Gerais, 31270010, Brazil.ORCID http://orcid.org/0000-0002-6269-8745
Cristiane Aparecida Menezes de PáduaCollege of Pharmacy, Universidade Federal de Minas Gerais, 6627 Antonio Carlos Ave, Belo Horizonte, Minas Gerais, 31270010, Brazil.ORCID http://orcid.org/0000-0001-7083-3188
Paula Lana de Miranda DrummondCollege of Pharmacy, Universidade Federal de Minas Gerais, 6627 Antonio Carlos Ave, Belo Horizonte, Minas Gerais, 31270010, Brazil.ORCID http://orcid.org/0000-0002-4639-7424
Jéssica Soares MaltaCollege of Pharmacy, Universidade Federal de Minas Gerais, 6627 Antonio Carlos Ave, Belo Horizonte, Minas Gerais, 31270010, Brazil.ORCID http://orcid.org/0000-0003-4610-393X
Adriano Max Moreira ReisCollege of Pharmacy, Universidade Federal de Minas Gerais, 6627 Antonio Carlos Ave, Belo Horizonte, Minas Gerais, 31270010, Brazil. amreis@outlook.com.ORCID http://orcid.org/0000-0002-0017-7338

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEmerging therapies for multiple myeloma (MM) have significantly improved patient outcomes extending survival and advancing treatment toward more targeted, effective, and less toxic approaches. However, the disease remains incurable.

objectivesAnalyze the therapeutic landscape of MM by evaluating drug candidates in clinical trials from 2014 to 2024.

methodsData were extracted from ClinicalTrials.gov (CTG) and Cortellis Drug Discovery Intelligence (CDDI), including active and completed studies with results on newly diagnosed and refractory MM. Joinpoint regression models estimated Annual Percent Changes (APCs) and Average Annual Percent Changes (AAPC). Data were examined by clinical trial characteristics, targeting strategies, and potential impact on treatment advancements.

resultsA total of 1091 trials from CDDI and 1947 from CTG were screened, yielding 365 studies eligible for detailed analysis. Phase I trials were the most common (n = 182; 49.9%), and biologic agents represented the majority of the investigational therapies (n = 251; 68.8%). Among intervention types, cell therapies were predominant (n = 171; 46.8%), with CAR-T products targeting BCMA (n = 107), CD19 (n = 16), and GPRC5D (n = 12) emerging as the most studied in recent years. Before the joinpoint, the number of active trials grew by 1.86% per year (95% CI: 1.67-2.06), corresponding to an average increase of 11.9 studies annually. After the joinpoint, growth accelerated to 3.69% per year (95% CI: 3.19-4.19), equivalent to 26.5 additional trials each year. Across the entire study period, the weighted average annual percentage change (AAPC) was 2.63%.

conclusionThe rise in MM clinical trials highlights a shift toward biologic therapies, particularly immunotherapies and gene therapies like CAR-T.

Indexed as

Antineoplastic AgentsMultiple MyelomaClinical Trials as TopicHumansAntineoplastic AgentsClinical trialsImmunotherapiesMultiple myelomaTherapeutics

Identifiers

PMID42098480
PMCPMC13354661

What OpenQuestion holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.