Diphtheria antitoxin 10,000units/10ml solution for injection ampoules
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Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 16 · Randomised trials: 5 · 1909–2026
Showing the 50 most relevant studies, sorted by most relevant.
Polonsky J, Hudu S, Uthman K, et al.
2026
Background During Nigeria’s largest recorded diphtheria outbreak, hospital capacity in Kano State was rapidly overwhelmed. Médecins Sans Frontières introduced home-based care (HBC) for patients with mild disease to prioritise facility-based care for severe cases. We assessed whether HBC was non-inferior to facility-based treatment in terms of mortality, sequelae, and household transmission. Methods We conducted a retrospective matched cohort study. Mild diphtheria cases treated between January 2023 and May 2024 were matched 1:1 by treatment modality (HBC or diphtheria treatment centre [DTC]) on sex, age group, vaccination status, and residence. Conditional logistic regression estimated the association between treatment modality and mortality, with robustness assessed through propensity score weighting, sensitivity analyses, and E-value computation. Findings Of 990 sampled patients, 678 (367 HBC, 311 DTC) were enrolled (68·5%). After adjustment, treatment modality was not independently associated with mortality (HBC vs. DTC: aOR 0·40, 95% CI 0·13–1·30), with similar estimates across sensitivity analyses (E-value 4·40). Clinical complications were the strongest predictor of death (aOR 23·1, 95% CI 1·73–307). Vaccination was protective (aOR 0·28, 95% CI 0·08– 0·94) and treatment delay of four or more days increased mortality (aOR 4·15, 95% CI 1·23–14·0). HBC was not associated with increased household transmission or long-term sequelae. Interpretation Vaccination and early treatment, rather than care setting, were the main determinants of survival. When supported by clinical triage and structured follow-up, decentralised care can be used to manage mild cases during diphtheria epidemics in settings with constrained hospital capacity. Funding Médecins Sans Frontières, West and Central Africa. Research in context Evidence before this study We searched PubMed and Google Scholar for articles published between January 1, 2000, and February 28, 2026, using combinations of the terms “diphtheria”, “outbreak”, “home-based care”, “outpatient”, “ambulatory”, “community care”, and “decentralised care”. We found no published studies evaluating any form of decentralised or home-based clinical management for diphtheria. The existing literature on diphtheria case management is confined to facility-based settings: outbreak reports from multiple affected countries describe hospital-based treatment with diphtheria antitoxin (DAT) and antibiotics, and a systematic review pooled epidemiological and clinical data from historical outbreaks. Decentralised care models have been evaluated for other epidemic-prone diseases, including a measles epidemic in the Democratic Republic of the Congo (DRC) where decentralised management reduced mortality among children, and Ebola virus disease outbreaks in DRC where decentralised treatment centres were piloted to improve geographic access, though with limited outcome data. No study has assessed whether patients with diphtheria can be safely managed outside hospital settings. Added value of this study No prior evaluation of home-based care for diphtheria has been published. Using a retrospective matched cohort design with 678 patients during the largest diphtheria outbreak in Africa in decades, we found no evidence that home-based care increased mortality, long-term complications, or household transmission compared with facility-based care, and acceptability was high among patients in both groups. The study also provides one of the largest datasets on household transmission of diphtheria in an urban epidemic setting, finding no evidence that home-based care increased secondary transmission, and showing that vaccination status of the index case was the main factor influencing spread within the household. Implications of all the available evidence Provided that triage is reliable, antibiotics are started promptly, and a functioning referral pathway exists, mild diphtheria can be managed safely at home during large epidemics. This approach preserves limited hospital and DAT resources for patients with moderate or severe disease, shortens treatment delays, and is acceptable to patients. Given ongoing outbreaks across West and Central Africa and persistent DAT supply constraints, decentralised care warrants inclusion in epidemic preparedness.
Abstract licence: CC BY
Muekara Friday Dugbor
Sreetechjournal Publication, 2024
R.J Collier
Toxicon, 2001
M Van der Wielen, P Van Damme, E Joossens, et al.
Vaccine, 2000
Fiona M Turnbull, Timothy C Heath, Bin B Jalaludin, et al.
Vaccine, 2000
Juhani Eskola, Joel Ward, Ron Dagan, et al.
The Lancet, 1999
Nasir Abdulrasheed, Lukman Lawal, A. B. Mogaji, et al.
Immunity, Inflammation and Disease, 2023
- Diphtheria
- Corynebacterium
- Diphtheria Antitoxin
Marta Prygiel, E. Mosiej, M. Polak, et al.
Toxins, 2024
- Diphtheria
- Diphtheria Toxin
- Corynebacterium
Javier Díez-Domingo, Maria V. Planelles, Jose M. Baldó, et al.
Current Therapeutic Research, 1998
Ian G Jones, Helen Tyrrell, Anthony Hill, et al.
Vaccine, 1998
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.