Lam, Tze Hau
Verzotto, Davide
Brahma, Purbita
Ng, Amanda Hui Qi
Hu, Ping
Schnell, Dan
Tiesman, Jay
Kong, Rong
Ton, Thi My Uyen
Li, Jianjun
Ong, May
Lu, Yang
Swaile, David
Liu, Ping
Liu, Jiquan
Nagarajan, Niranjan
Funding for this research was provided by:
Agency for Science, Technology and Research (APG2013/032)
Procter and Gamble
Article History
Received: 28 May 2018
Accepted: 2 November 2018
First Online: 29 November 2018
Ethics approval and consent to participate
: The study was conducted and all samples were collected by PRICEPTS Inc. (PRICE Product Testing Services Incorporated) in Manila with approval from the Procter & Gamble Singapore Innovation Center (Singapore) Institutional Review Board and in accordance with the World Medical Association Declaration of Helsinki (1996 amendment). ICH Guidelines for Good Clinical Practice (GCPs) were followed, and voluntary informed consent was provided with the approval of the Research Ethics Board of P&G. This clinical investigation complied with STROBE guidelines for observational human studies. Mothers who agreed to have their children participate in this study signed an informed consent form and teenagers who agreed to participate signed an assent form.
: Not applicable.
: Several co-authors (L.Y. D.S. P.L. J.L. P.B. P.H. J.T. R.K. T.T. M.O.) contributed to and/or conducted this study while being employed by the Procter & Gamble Company. These co-authors may own stock in the company, but direct financial gain or loss from the publication of this manuscript is not anticipated. Under a requirement of employment obligations of the Procter & Gamble Company to maintain confidentiality, these co-authors cannot declare patent activity.
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