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"Vyepti EPAR". European Medicines Agency (EMA). 11 November 2021. Diarsipkan dari versi aslinya tanggal 8 June 2022. Diakses tanggal 8 June 2022. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
World Health Organization (2017). "International nonproprietary names for pharmaceutical substances (INN): recommended INN: list 77". WHO Drug Information. 31 (1). hdl:10665/330984.
Dodick DW, Goadsby PJ, Silberstein SD, Lipton RB, Olesen J, Ashina M, et al. (November 2014). "Safety and efficacy of ALD403, an antibody to calcitonin gene-related peptide, for the prevention of frequent episodic migraine: a randomised, double-blind, placebo-controlled, exploratory phase 2 trial". The Lancet. Neurology. 13 (11): 1100–1107. doi:10.1016/S1474-4422(14)70209-1. PMID25297013. S2CID206161999.
Dodick DW, Goadsby PJ, Silberstein SD, Lipton RB, Olesen J, Ashina M, et al. (November 2014). "Safety and efficacy of ALD403, an antibody to calcitonin gene-related peptide, for the prevention of frequent episodic migraine: a randomised, double-blind, placebo-controlled, exploratory phase 2 trial". The Lancet. Neurology. 13 (11): 1100–1107. doi:10.1016/S1474-4422(14)70209-1. PMID25297013. S2CID206161999.
"Vyepti". Therapeutic Goods Administration (TGA). 24 June 2021. Diarsipkan dari versi aslinya tanggal 6 September 2021. Diakses tanggal 6 September 2021.
"AusPAR: Eptinezumab". Therapeutic Goods Administration (TGA). 3 March 2022. Diarsipkan dari versi aslinya tanggal 24 March 2022. Diakses tanggal 23 March 2022.
"Vyepti". Therapeutic Goods Administration (TGA). 24 June 2021. Diarsipkan dari versi aslinya tanggal 6 September 2021. Diakses tanggal 6 September 2021.
"AusPAR: Eptinezumab". Therapeutic Goods Administration (TGA). 3 March 2022. Diarsipkan dari versi aslinya tanggal 24 March 2022. Diakses tanggal 23 March 2022.
"Vyepti EPAR". European Medicines Agency (EMA). 11 November 2021. Diarsipkan dari versi aslinya tanggal 8 June 2022. Diakses tanggal 8 June 2022. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.