Evidence map›Paper›PMID 37983978›Full record

Trial reportClinical pharmacology and therapeutics2024

A Dose-Finding Study to Guide Use of Verapamil as an Adjunctive Therapy in Tuberculosis.

Chandrasekaran Padmapriyadarsini, John D Szumowski, Nabila Akbar, Prema Shanmugasundaram, Anilkumar Jain, Marasamy Bathragiri, Manoranjan Pattnaik, Jyotirmayee Turuk, Ramesh Karunaianantham, Senthilkumar Balakrishnan and 11 more

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in Clinical pharmacology and therapeutics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 15% of its field
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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Verapamil and its metabolite norverapamil inhibit theProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Host-directed therapy for tuberculosis.European journal of medical research · 2025
    Review
  6. Review
  7. Review
  8. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 12 institutions in 3 countries.

Chandrasekaran Padmapriyadarsini *National Institute for Research in Tuberculosis, Chennai, India.ORCID 0000-0002-1324-4595
John D Szumowski *Division of HIV, Infectious Diseases and Global Medicine, Department of Medicine, Zuckerberg San Francisco General Hospital and Trauma Center, University of California San Francisco, San Francisco, California, USA.ORCID 0000-0002-0287-9704
Nabila AkbarNational Institute for Research in Tuberculosis, Chennai, India.
Prema ShanmugasundaramNational Institute for Research in Tuberculosis, Chennai, India.
Anilkumar JainNational Institute of Tuberculosis and Respiratory Diseases, New Delhi, India.
Marasamy BathragiriGovernment Kilpauk Medical College and Hospital, Chennai, India.
Manoranjan PattnaikDepartment of Pulmonary Medicine, SCB Medical College, Cuttack, India.ORCID 0000-0002-9955-0373
Jyotirmayee TurukRegional Medical Research Centre, Bhubaneswar, India.ORCID 0000-0002-8821-6097
Ramesh KarunaiananthamNational Institute for Research in Tuberculosis, Chennai, India.ORCID 0000-0002-4206-5609
Senthilkumar BalakrishnanNational Institute for Research in Tuberculosis, Chennai, India.ORCID 0009-0006-3075-7161
Sanghamitra PatiRegional Medical Research Centre, Bhubaneswar, India.
A K Hemanth KumarNational Institute for Research in Tuberculosis, Chennai, India.
Manoj Kumar RathoreSITEC Labs, Navi Mumbai, India.ORCID 0009-0002-3041-4741
Jegadeesh RajaSITEC Labs, Navi Mumbai, India.ORCID 0009-0009-5770-0642
K Raghu NaiduSITEC Labs, Navi Mumbai, India.ORCID 0009-0008-2174-5016
John HornDepartment of Pharmacy, University of Washington, Seattle, Washington, USA.ORCID 0000-0003-4525-4250
Laura WhitworthMolecular Immunity Unit, Department of Medicine, Cambridge Institute of Therapeutic Immunology and Infectious Diseases, University of Cambridge, Cambridge, UK.ORCID 0000-0002-8232-4601
Roger SewellTrinity College, Cambridge, UK.ORCID 0000-0003-4267-7055
Lalita RamakrishnanMolecular Immunity Unit, Department of Medicine, Cambridge Institute of Therapeutic Immunology and Infectious Diseases, University of Cambridge, Cambridge, UK.ORCID 0000-0003-0692-5533
Soumya SwaminathanNational Institute for Research in Tuberculosis, Chennai, India.ORCID 0009-0004-2233-7250
Paul H EdelsteinMolecular Immunity Unit, Department of Medicine, Cambridge Institute of Therapeutic Immunology and Infectious Diseases, University of Cambridge, Cambridge, UK.ORCID 0000-0002-4069-5279
National Institute of Research in Tuberculosis · INIndian Navy · INMRC Laboratory of Molecular Biology · GBRegional Medical Research Centre · INGovernment Kilpauk Medical College · INLRS Institute of Tuberculosis and Respiratory Diseases · INM S Swaminathan Research Foundation · INSan Francisco General Hospital · USSriram Chandra Bhanja Medical College Hospital · INTrinity College London · GBUniversity of Cambridge · GBUniversity of Washington · US

Funding

HOST DEFENSE TRAINING IN ALLERGY AND INFECTIOUS DISEASEST32AI007044 · NIAID · UNIVERSITY OF WASHINGTON · PI DAVID Neal FREDRICKS · 1985 to 2026
$14.6M
Host Responses to Mycobacterium Infection in ZebrafishR01AI054503 · NIAID · UNIVERSITY OF WASHINGTON · PI LALITA RAMAKRISHNAN · 2003 to 2026
$4.4M
NIAID NIH HHS R01 AI054503NIAID NIH HHS T32 AI007044Wellcome Trust 223103
6 · The paper itself

Abstract

Induction of mycobacterial efflux pumps is a cause of Mycobacterium tuberculosis (Mtb) drug tolerance, a barrier to shortening antitubercular treatment. Verapamil inhibits Mtb efflux pumps that mediate tolerance to rifampin, a cornerstone of tuberculosis (TB) treatment. Verapamil's mycobacterial efflux pump inhibition also limits Mtb growth in macrophages in the absence of antibiotic treatment. These findings suggest that verapamil could be used as an adjunctive therapy for TB treatment shortening. However, verapamil is rapidly and substantially metabolized when co-administered with rifampin. We determined in a dose-escalation clinical trial of persons with pulmonary TB that rifampin-induced clearance of verapamil can be countered without toxicity by the administration of larger than usual doses of verapamil. An oral dosage of 360 mg sustained-release (SR) verapamil given every 12 hours concomitantly with rifampin achieved median verapamil exposures of 903.1 ng.h/mL (area under the curve (AUC)

Indexed as

Mycobacterium tuberculosisTuberculosisAntitubercular AgentsHumansRifampinVerapamilAntitubercular AgentsnorverapamilRifampinVerapamil

Identifiers

PMID37983978
PMCPMC7615557
OpenAlexW4388852212

What OpenQuestion holds

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Registered trials

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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.