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Nutritional Content and a Phase - I Safety Clinical Trial of a Herbal-Nutritional Supplement (Imuniti) With Putative Immune-Modulating Properties

Bibliographic Data

ID20346286
AuthorsPulok K Mukherjee (0000-0003-2921-8882, South African Medical Research Council), MG Matsabisa, Mamello Sekhoacha (0000-0001-5090-0259, South African Medical Research Council), MP Sekhoacha, O Ibrahim, Olayinka Rasheed Ibrahim (0000-0002-2621-6593), Pravikrishnen Moodley (0000-0002-9946-8783), M Faber, M N Faber (South African Medical Research Council)
Year2012
Volume9
Issue3S
Pages19-23
Publication date2012-09-27
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueAfrican Journal of Traditional Complementary and Alternative Medicines (JOURNAL)
Journal identifiersISSN: 0189-6016 • E-ISSN: 2505-0044
PublisherAfrican Journals Online (AJOL) (PUBLISHER)
DOI10.4314/ajtcam.v9i3s.3
PMID23983351
OpenAlexW1976622514
LanguageEN
Citations received1
References cited1

The relationship between HIV and AIDS and poor nutrition has been well established. Poor nutrition hastens the progression of HIV infection to AIDS. The rising pandemic of HIV and AIDS and high toxicity associated with anti-retroviral use are major factors that have compelled research to explore traditional herbal medicines as potential alternatives or supplements to anti-retroviral agents. A Phase I clinical trial was conducted on IMUNITI Wellness Pack, a herbal product with putative immune-modulating properties. The product is a combination of 7 herbal preparations, minerals, vitamins, and a specially formulated soya-maize meal porridge and a bottle of water purifier. The aim was to evaluate the safety and tolerability of IMUNITI, with a purpose of developing it for use in HIV-infected patients. The phase I study was conducted at the MRC clinic in Botha's hill and the study lasted 5 weeks from date of participant dosing. The study was a randomised blinded placebo-controlled phase I clinical trial conducted on 48 healthy males. The participants were randomly divided into 4 groups of 12. The 3 groups received different escalating doses of IMUNITI while the forth group received placebo tablets. Participants consumed IMUNITI daily for a period of 5 weeks. Assessments were done at baseline, week 1 and week 5 to determine the safety parameters in all participants. In this study, IMUNITI did not show any safety concerns. In all study participants, there were no significant changes above the upper limit of the reference ranges of the laboratory tests for full blood count, INR, renal and biochemical safety parameters. IMUNITI was well tolerated. Furthermore, the nutritional content analysis of IMUNITI showed that it is a high kilojoule, high protein content product which contains a mixture of sugars, vitamins, traces of calcium, phosphorus and minerals

Alternative medicine · Biology · Dietary supplement · Herbal supplement · Immune system · Pathology · Traditional medicine · Drug-Induced Hepatotoxicity and Protection · Folate and B Vitamins Research · Inflammatory Bowel Disease · Medicine · Food Science · Immunology

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Unique citing works1
Citations per year0,07
Citation span2012 - 2012 (1)
Citation velocityhistorical
Highly citedNo

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