Condition category
Infections and Infestations
Date applied
28/11/2019
Date assigned
13/12/2019
Last edited
13/12/2019
Prospective/Retrospective
Retrospectively registered
Overall trial status
Completed
Recruitment status
No longer recruiting
Publication status
Results

Plain English Summary

Background and study aims:
Leprosy and tuberculosis (TB) are caused by infection with two types of Mycobacterium bacteria. Leprosy can damage nerves resulting in loss of sensation in the fingers and toes. This can result in damage and loss of the fingers and toes because people cannot feel when they have injured them or when there is infection. Leprosy can be treated with antibiotics and the number of cases worldwide has reduced significantly from the 1980s, when there were millions of people affected. TB mainly affects the lungs and still causes more than a million deaths per year worldwide. It can be prevented to some extent with the BCG vaccine (but protection varies greatly between countries) and treated with antibiotics, although there are strains that are resistant to drug treatment.
This trial started in 1985. It was designed to investigate two questions. The first was whether giving a second dose of the BCG vaccine would give people more protection against TB and leprosy than just one. The second question was whether adding killed leprosy bacteria to the BCG vaccine would increase protection against leprosy. The trial took place in Karonga District, a rural area in northern Malawi, as part of a large study of leprosy and TB which had begun in 1979, called the Lepra Evaluation Project.
Recruitment into the original trial took place between early 1986 and late 1989, and the first results were analysed and published in 1996, showing that repeating BCG vaccination gave approximately an additional 50% protection against leprosy but no significant protection against TB. There were suggestions in the results that the vaccines might give some protection against TB among those who were vaccinated at young age and that the vaccines might be providing protection against extrapulmonary TB (in which the disease is outside the lungs), but the numbers of cases in these groups were not large enough for the results to be convincing. In addition there was some evidence that the BCG vaccine might be associated with increased risk of TB among individuals who were HIV-positive.
The aim of the current study is to follow up on the people who participated in the original trial, now that more than 30 years have passed and it will be possible to investigate the long-term effects of the vaccinations in different groups of participants, such as those who were vaccinated at a young age and those who subsequently became HIV-positive.

Who can participate?
All individuals aged between 3 months and 70 years of age in 1985 were eligible to participate in the original trial.

What does the study involve?
In the original study, more than 120,000 people were randomised in the following way. If they had no BCG vaccination scar, they were randomly allocated to receive plain BCG vaccine or BCG vaccine combined with killed leprosy bacteria. If they had a BCG vaccination scar, they were randomly allocated to receive either a second dose of BCG vaccine, a second dose of BCG vaccine combined with killed leprosy bacteria or a placebo (an injection with no vaccine). The entire population was then followed up and all cases of leprosy and TB were reported to the trial team.

What are the possible benefits and risks of participating?
All participants received at least one dose of BCG vaccine, which had already been shown to provide 50% protection against leprosy. Many of the participants received a second dose of BCG with or without killed leprosy bacteria, which might give them additional protection. Repeated BCG vaccination was policy in several countries at the time and known to be safe. The addition of killed leprosy bacteria to BCG had been shown to be safe in trials in Norway and Malawi.

Where is the study run from?
The trial headquarters were in Chilumba, a village in Karonga District, Malawi, which had been the headquarters of the Lepra Evaluation Project (LEP) since 1979. The LEP and the trial were closely linked to a research team at the London School of Hygiene and Tropical Medicine (UK). The Malawi activities of the trial are now carried out within the Malawi Epidemiology and Intervention Research Unit (MEIRU), which combines field research in Karonga District with parallel projects in an urban area in the capital city, Lilongwe.

When is the study starting and how long is it expected to run for?
January 1983 to December 2018

Who is funding the study?
The original trial was funded by the British Leprosy Relief Association (LEPRA), the International Federation of anti-Leprosy organisations (ILEP) and the Immunology of Leprosy (IMMLEP) Component of the WHO/World Bank/UNDP Tropical Disease Research Programme. The follow-up after 1996 was funded largely by the Wellcome Trust (UK). The current follow-up analyses are funded by the Bill & Melinda Gates Foundation (USA).

Who is the main contact?
Professor Paul Fine, paul.fine@lshtm.ac.uk

Trial website

Contact information

Type

Scientific

Primary contact

Prof Paul Fine

ORCID ID

Contact details

London School of Hygiene and Tropical Medicine (LSHTM)
Keppel Street
London
WC1E 7HT
United Kingdom
+44 (0)207 927 2219
paul.fine@lshtm.ac.uk

Additional identifiers

EudraCT number

Nil known

ClinicalTrials.gov number

Nil known

Protocol/serial number

N/A

Study information

Scientific title

Randomised controlled trial of the efficacy of repeat BCG vaccine, or BCG plus killed M leprae vaccine, in the prevention of clinical leprosy and tuberculosis, in the general population of Karonga District, northern Malawi

Acronym

KPT (Karonga Prevention Trial)

Study hypothesis

1. Does repeated BCG vaccination give greater protection against leprosy and tuberculosis than a single vaccination?
2. Does a combined vaccine with BCG plus killed M leprae bacilli provide greater protection against leprosy than does BCG vaccine alone?
3. Is the protection induced by either of these vaccines greatest in those vaccinated at youngest ages?
4. Is the protection induced by either of these vaccines greatest among those without tuberculin reactivity at time of vaccination?
5. Does the protection induced by either of these vaccines decline with time since vaccination?
6. Does the protection induced by repeated BCG against tuberculosis differ as a function of the genetic lineage of M tuberculosis?
7. Is the protection induced by repeat BCG different by type of tuberculosis (pulmonary or glandular)?
8. Is the protection induced by these vaccines lower in individuals who are HIV-positive at time of diagnosis compared to those HIV-negative at diagnosis?

Ethics approval

1. Approved 16/09/1985, London School of Hygiene and Tropical Medicine Ethical Committee (Keppel St, London WC1E 7HT; Telephone number not provided as it is likely to be out of date; No email address), no reference number
2. Protocol amendment approved 22/12/1986, London School of Hygiene and Tropical Medicine Ethical Committee (Keppel St, London WC1E 7HT; Telephone number not provided as it is likely to be out of date; No email address), ref: 110
3. Update to cover epidemiology of mycobacterial and HIV infections in Northern Malawi approved 01/08/2001, London School of Hygiene and Tropical Medicine Ethics Committee (Keppel St, London WC1E 7HT; No telephone number; No email address), ref: 745A

The trial protocol was approved in 1985 by the Health Sciences Research Committee of the Malawi Ministry of Health, the Standing Committee on Research in Human Subjects of WHO, and the Ethics Committee of the London School of Hygiene and Tropical Medicine. Continued ascertainment of cases has been approved in the context of a series of subsequent studies.

Study design

Randomized double-blind placebo-controlled trial

Primary study design

Interventional

Secondary study design

Randomised controlled trial

Trial setting

Community

Trial type

Prevention

Patient information sheet

No participant information sheet available.

Condition

Leprosy and tuberculosis

Intervention

The trial was explained in public meetings with village headmen and to each household as they were visited.

Individuals with a BCG scar were randomised (by vaccine vial*) to receive either Glaxo's standard commercialised BCG vaccine, BCG + 6 x 10(8) killed Mycobacterium leprae vaccine (an investigational vaccine produced by Wellcome Laboratories) or placebo.
Individuals with no BCG scar were randomised (by vaccine vial) to receive either BCG vaccine, or BCG + 5 x 10(7) killed M leprae vaccine, or BCG + 6 x 10(8) killed M leprae vaccine
The placebo consisted of the dextran matrix of BCG vaccine, minus the bacilli. All vaccines were given intradermally. Vaccine vials within each (scar-negative and scar-positive) group were identical, and coded independently by WHO-appointed trial monitor.

* Small group randomisation was used because vaccine vials were multidose (1 - 11 doses per vial).

Intervention type

Biological/Vaccine

Phase

Phase III

Drug names

1. BCG (Bacillus Calmette-Guerin) vaccine, produced by Glaxo
2. Killed Mycobacterium leprae vaccine, produced by Wellcome Laboratories
3. Placebo produced by Glaxo (dextran matrix of BCG vaccine)

Primary outcome measure

1. Presence of clinical leprosy, confirmed as certain or probable by an algorithm based upon clinical findings and biopsy, with onset at any time after vaccination until end of 2018. The algorithm for diagnostic certainty is described in detail in Pönnighaus et al, 1987.
2. Presence of clinical tuberculosis, confirmed as certain or probable based on sputum smear, sputum culture, biopsy and GeneXpert, and ascertained at least 6 months after vaccination until end of 2018:
2.1. Pulmonary tuberculosis was considered certain if culture-positive or GeneXpert-positive plus at least one other specimen positive on culture or GeneXpert or microscopy and probable if culture- or GeneXpert- or microscopy-positive but not fulfilling criteria for certain, excluding those with only a single scanty smear (i.e. fewer than 10 bacilli per 100 fields)
2.2. Extrapulmonary tuberculosis was considered certain if confirmed by histology or microscopy or culture/GeneXpert and probable if histology suggestive or clinical lymph node tuberculosis. Note that since only 2 of 96 extrapulmonary TB are 'probable' in new data, it was decided to restrict to histologically or microscopy or culture/GeneXpert confirmed.

Secondary outcome measures

1. Time since vaccination measured from the date of vaccination to the date when the individual was first seen by project staff with clinical signs (for leprosy) or to the earliest of the date of first diagnostic specimen, or of registration or of start of treatment (for tuberculosis)
2. Tuberculin status at vaccination assessed with RT23 tuberculin (produced by Danish Statens Serum Institut) 2 IU injected intradermally into the volar surface of the forearm. Induration was measured along and across arm after 48 – 72 hours. Average diameter was used in analyses.
3. M tuberculosis lineage assessed using assessed by whole genome sequence, if available, or, if unavailable, by restriction fragment length polymorphism, or spoligotype
4. HIV status assessed by algorithm based upon rapid tests. Individuals considered HIV negative if last negative report was <1 year before or any time after key date and as HIV positive if first positive report was any time before and up to 1 year after key date (unless known HIV negative at the key date). The participant's HIV status was classed as unknown otherwise. Self reports of HIV positivity or ART use were accepted as evidence of HIV positivity


Overall trial start date

01/01/1983

Overall trial end date

31/12/2018

Reason abandoned (if study stopped)

Eligibility

Participant inclusion criteria

1. Healthy
2. Aged over 3 months
3. Born after 1914
4. No history of leprosy or tuberculosis

Participant type

All

Age group

All

Gender

Both

Target number of participants

120,000

Participant exclusion criteria

1. Aged under 3 months
2. Born before 1914
3. Evidence of past or current leprosy or tuberculosis
4. Severe malnutrition or other severe illness

Recruitment start date

09/01/1986

Recruitment end date

30/11/1989

Locations

Countries of recruitment

Malawi

Trial participating centre

Karonga Prevention Study
Chilumba
-
Malawi

Sponsor information

Organisation

London School of Hygiene and Tropical Medicine

Sponsor details

Keppel Street
London
WC1E 7HT
United Kingdom
44 (0) 207-636-8636
postmaster@lshtm.ac.uk

Sponsor type

University/education

Website

http://www.lshtm.ac.uk

Funders

Funder type

Charity

Funder name

British Leprosy Relief Association (LEPRA)

Alternative name(s)

Funding Body Type

Funding Body Subtype

Location

Funder name

International Federation of Ant-Leprosy Associations (ILEP)

Alternative name(s)

Funding Body Type

Funding Body Subtype

Location

Funder name

IMMLEP Component of WHO/TDR

Alternative name(s)

Funding Body Type

Funding Body Subtype

Location

Funder name

Bill & Melinda Gates Foundation

Alternative name(s)

Funding Body Type

Funding Body Subtype

Location

Funder name

The Wellcome Trust

Alternative name(s)

Funding Body Type

Funding Body Subtype

Location

Results and Publications

Publication and dissemination plan

The design and initial results of the trial have already been published. The current intention is to carry out a 30-year follow-up of the trial population and publish the results in 2020.

IPD sharing statement:
The datasets generated during and/or analysed during the current study will be available upon request from Datacompass at LSHTM. Researchers should contact Paul Fine (paul.fine@lshtm.ac.uk). The datasets will be in CSV format sent by secure file transfer and will be available from one month after publication for one year minimum. Access will be dependent on an explicit collaborator agreement. Analyses relating to effectiveness of vaccines against leprosy and/or tuberculosis will be enabled. Participants consented verbally to trial participation. The data will be anonymised – no names, addresses, GPS coordinates, or precise birth dates will be included in shared data.
Any sharing agreement will include requirements (a) to obtain approval from original investigators and MEIRU of analyses in any publication based upon the shared data (b) for full acknowledgment and recognition of original investigators and MEIRU in any subsequent publication and (c) against onward sharing of the data provided without explicit permission from investigators and MEIRU.

Intention to publish date

31/12/2020

Participant level data

Available on request

Basic results (scientific)

Publication list

1998 protocol in https://doi.org/10.1016/0035-9203(88)90003-X (added 29/11/2019)
1993 methods in https://www.ncbi.nlm.nih.gov/pubmed/8127221 (added 29/11/2019)
1996 initial results in https://www.ncbi.nlm.nih.gov/pubmed/8691924 (added 29/11/2019)


Publication citations

Additional files

Editorial Notes

12/12/2019: Trial's existence confirmed by the Malawi Ministry of Health.