Biblioteca de investigación
Cómo leer un estudio. Qué significa nuestra escala de evidencia. Un conjunto curado de referencias.
Cómo leer investigación sobre péptidos
Interpretar estudios sobre péptidos requiere distinguir entre datos preclínicos y humanos, entender los tamaños muestrales y reconocer cuándo un titular exagera un hallazgo.
Nuestra escala de evidencia
- Evidencia humana sólida
Respaldada por múltiples ensayos clínicos aleatorizados amplios en humanos y, cuando aplica, por la aprobación de las principales agencias regulatorias.
- Evidencia humana moderada
Apoyada por ensayos en humanos, pero de tamaño, duración o replicación limitadas. Puede estar aprobada para indicaciones relacionadas pero no idénticas.
- Evidencia humana inicial
Estudios humanos de pequeña escala, datos observacionales o experiencia fuera de indicación. Persiste una incertidumbre considerable.
- Evidencia preclínica
Datos procedentes de modelos animales, estudios celulares o reportes anecdóticos comunitarios. Sin evidencia humana controlada.
Referencias
- [1]
Efficacy and safety of a novel dual GIP and GLP-1 receptor agonist tirzepatide in patients with type 2 diabetes (SURPASS-1) — Rosenstock J, Wysham C, Frías JP, et al.
The Lancet. 2021. RCT — Source
- [2]
Tirzepatide versus semaglutide once weekly in patients with type 2 diabetes (SURPASS-2) — Frías JP, Davies MJ, Rosenstock J, et al.
New England Journal of Medicine. 2021. RCT — Source
- [3]
Tirzepatide once weekly for the treatment of obesity (SURMOUNT-1) — Jastreboff AM, Aronne LJ, Ahmad NN, et al.
New England Journal of Medicine. 2022. RCT — Source
- [4]
Continued treatment with tirzepatide for maintenance of weight reduction in adults with obesity (SURMOUNT-4) — Aronne LJ, Sattar N, Horn DB, et al.
JAMA. 2024. RCT — Source
- [5]
FDA Prescribing Information — MOUNJARO (tirzepatide) injection — U.S. Food and Drug Administration
2022. guideline — Source
- [6]
FDA Prescribing Information — ZEPBOUND (tirzepatide) injection — U.S. Food and Drug Administration
2023. guideline — Source
- [7]
Mounjaro (tirzepatide) — European Public Assessment Report (EPAR) — European Medicines Agency
2022. guideline — Source
- [8]
Tirzepatide once weekly for the treatment of obesity in people with type 2 diabetes (SURMOUNT-2) — Garvey WT, Frías JP, Jastreboff AM, et al.
The Lancet. 2023. RCT — Source
- [9]
Tirzepatide is an imbalanced and biased dual GIP and GLP-1 receptor agonist — Willard FS, Douros JD, Gabe MBN, et al.
JCI Insight. 2020. preclinical — Source
- [10]
Once-Weekly Semaglutide in Adults with Overweight or Obesity (STEP 1) — Wilding JPH, Batterham RL, Calanna S, et al.
New England Journal of Medicine. 2021. RCT — Source
- [11]
Effect of Continued Weekly Subcutaneous Semaglutide vs Placebo on Weight Loss Maintenance in Adults With Overweight or Obesity: The STEP 4 Randomized Clinical Trial — Rubino D, Abrahamsson N, Davies M, et al.
JAMA. 2021. RCT — Source
- [12]
Two-year effects of semaglutide in adults with overweight or obesity: the STEP 5 trial — Garvey WT, Batterham RL, Bhatta M, et al.
Nature Medicine. 2022. RCT — Source
- [13]
Effect of Weekly Subcutaneous Semaglutide vs Daily Liraglutide on Body Weight in Adults With Overweight or Obesity Without Diabetes: The STEP 8 Randomized Clinical Trial — Rubino DM, Greenway FL, Khalid U, et al.
JAMA. 2022. RCT — Source
- [14]
Semaglutide and Cardiovascular Outcomes in Patients with Type 2 Diabetes (SUSTAIN-6) — Marso SP, Bain SC, Consoli A, et al.
New England Journal of Medicine. 2016. RCT — Source
- [15]
Semaglutide and Cardiovascular Outcomes in Obesity without Diabetes (SELECT) — Lincoff AM, Brown-Frandsen K, Colhoun HM, et al.
New England Journal of Medicine. 2023. RCT — Source
- [16]
Effect of Additional Oral Semaglutide vs Sitagliptin on Glycated Hemoglobin in Adults With Type 2 Diabetes Uncontrolled With Metformin Alone or With Sulfonylurea: The PIONEER 3 Randomized Clinical Trial — Rosenstock J, Allison D, Birkenfeld AL, et al.
JAMA. 2019. RCT — Source
- [17]
Semaglutide in Patients with Heart Failure with Preserved Ejection Fraction and Obesity (STEP-HFpEF) — Kosiborod MN, Abildstrøm SZ, Borlaug BA, et al.
New England Journal of Medicine. 2023. RCT — Source
- [18]
Effects of Semaglutide on Chronic Kidney Disease in Patients with Type 2 Diabetes (FLOW) — Perkovic V, Tuttle KR, Rossing P, et al.
New England Journal of Medicine. 2024. RCT — Source
- [19]
FDA Prescribing Information — OZEMPIC (semaglutide) injection — U.S. Food and Drug Administration
2017. guideline — Source
- [20]
FDA Prescribing Information — WEGOVY (semaglutide) injection — U.S. Food and Drug Administration
2021. guideline — Source
- [21]
FDA Prescribing Information — RYBELSUS (semaglutide) tablets — U.S. Food and Drug Administration
2019. guideline — Source
- [22]
Ozempic (semaglutide) — European Public Assessment Report (EPAR) — European Medicines Agency
2018. guideline — Source
- [23]
Wegovy (semaglutide) — European Public Assessment Report (EPAR) — European Medicines Agency
2022. guideline — Source
- [24]
Discovery of the Once-Weekly Glucagon-Like Peptide-1 (GLP-1) Analogue Semaglutide — Lau J, Bloch P, Schäffer L, et al.
Journal of Medicinal Chemistry. 2015. preclinical — Source
- [25]
Effects of tesamorelin (TH9507), a growth hormone–releasing factor analog, in HIV-infected patients with excess abdominal fat — Falutz J, Allas S, Blot K, et al.
New England Journal of Medicine. 2007. RCT — Source
- [26]
Long-term safety and effects of tesamorelin, a growth hormone-releasing factor analogue, in HIV patients with abdominal fat accumulation — Falutz J, Potvin D, Mamputu JC, et al.
AIDS. 2010. RCT — Source
- [27]
Effects of tesamorelin on visceral fat and liver fat in HIV-infected patients with abdominal fat accumulation: a randomized clinical trial — Stanley TL, Feldpausch MN, Oh J, et al.
JAMA. 2014. RCT — Source
- [28]
Effects of tesamorelin on non-alcoholic fatty liver disease in HIV: a randomised, double-blind, multicentre trial — Stanley TL, Fourman LT, Feldpausch MN, et al.
The Lancet HIV. 2019. RCT — Source
- [29]
FDA Prescribing Information — EGRIFTA / EGRIFTA SV (tesamorelin) for injection — U.S. Food and Drug Administration
2010. guideline — Source
- [30]
Growth hormone-releasing hormone (GHRH)(1-29)NH2 for treatment of GH deficiency in adults: a randomized, double-blind, placebo-controlled trial — Walker RF, Codd EE, Barone FC, et al.
Journal of Clinical Endocrinology & Metabolism. 1994. RCT — Source
- [31]
Once daily subcutaneous growth hormone-releasing hormone therapy accelerates growth in growth hormone-deficient children during the first year of therapy — Thorner MO, Rochiccioli P, Colle M, et al.
Journal of Clinical Endocrinology & Metabolism. 1996. RCT — Source
- [32]
FDA history — GEREF (sermorelin acetate) for injection (approval 1990, withdrawn 2008) — U.S. Food and Drug Administration
2008. guideline — Source
- [33]
Sermorelin: a better approach to management of adult-onset growth hormone insufficiency? — Prakash A, Goa KL
BioDrugs. 1999. review — Source
- [34]
Prolonged stimulation of growth hormone (GH) and insulin-like growth factor I secretion by CJC-1295, a long-acting analog of GH-releasing hormone, in healthy adults — Teichman SL, Neale A, Lawrence B, et al.
Journal of Clinical Endocrinology & Metabolism. 2006. RCT — Source
- [35]
Pulsatile secretion of growth hormone (GH) persists during continuous stimulation by CJC-1295, a long-acting GH-releasing hormone analog — Ionescu M, Frohman LA
Journal of Clinical Endocrinology & Metabolism. 2006. RCT — Source
- [36]
Once-daily administration of CJC-1295, a long-acting growth hormone-releasing hormone (GHRH) analog, normalizes growth in the GHRH knockout mouse — Alba M, Fintini D, Sagazio A, et al.
American Journal of Physiology - Endocrinology and Metabolism. 2006. preclinical — Source
- [37]
Ipamorelin, the first selective growth hormone secretagogue — Raun K, Hansen BS, Johansen NL, et al.
European Journal of Endocrinology. 1998. preclinical — Source
- [38]
Pharmacokinetic-pharmacodynamic modeling of ipamorelin, a growth hormone releasing peptide, in human volunteers — Gobburu JVS, Agersø H, Jusko WJ, Ynddal L
Pharmaceutical Research. 1999. RCT — Source
- [39]
Ipamorelin, a growth hormone secretagogue, does not reduce postoperative ileus in patients undergoing bowel resection: results of a phase 2, randomized, double-blind, placebo-controlled trial — Beck DE, Sweeney WB, McCarter MD, Ipamorelin 2201 Study Group
International Journal of Colorectal Disease. 2014. RCT — Source
- [40]
Ipamorelin, a novel and selective growth hormone secretagogue: preclinical characterization — Andersen NB, Malmlöf K, Johansen PB, Andreassen TT, Ørtoft G, Oxlund H
Growth Hormone & IGF Research. 2001. preclinical — Source
- [41]
Stable gastric pentadecapeptide BPC 157: novel therapy in gastrointestinal tract — Sikiric P, Seiwerth S, Rucman R, et al.
Current Pharmaceutical Design. 2010. review — Source
- [42]
The promoting effect of pentadecapeptide BPC 157 on tendon healing involves tendon outgrowth, cell survival, and cell migration — Chang CH, Tsai WC, Lin MS, Hsu YH, Pang JHS
Journal of Applied Physiology. 2011. preclinical — Source
- [43]
BPC 157 and Standard Angiogenic Growth Factors — Gastrointestinal Tract Healing, Lessons from Tendon, Ligament, Muscle and Bone Healing — Seiwerth S, Milavic M, Vukojevic J, et al.
Frontiers in Pharmacology. 2019. review — Source
- [44]
Stable gastric pentadecapeptide BPC 157 in the treatment of colitis and ischemia and reperfusion in rats: new insights — Sikiric P, Rucman R, Turkovic B, et al.
World Journal of Gastroenterology. 2018. preclinical — Source
- [45]
Thymosin beta 4: actin-sequestering protein moonlights to repair injured tissues — Goldstein AL, Hannappel E, Kleinman HK
Trends in Molecular Medicine. 2005. review — Source
- [46]
Thymosin beta4 accelerates wound healing — Malinda KM, Sidhu GS, Mani H, et al.
Journal of Investigative Dermatology. 1999. preclinical — Source
- [47]
Thymosin beta4: structure, function, and biological properties supporting current and future clinical applications — Crockford D, Turjman N, Allan C, Angel J
Annals of the New York Academy of Sciences. 2010. review — Source
- [48]
Preclinical safety assessment of Thymosin β4 for the treatment of patients with damaged heart tissue — Ruff D, Crockford D, Girardi G, Zhang Y
Annals of the New York Academy of Sciences. 2010. preclinical — Source
- [49]
World Anti-Doping Agency (WADA) Prohibited List — S2 peptide hormones, growth factors, related substances, and mimetics — World Anti-Doping Agency
2024. guideline — Source
- [50]
A tripeptide in human serum which prolongs survival of normal liver cells and stimulates growth in neoplastic liver — Pickart L, Thaler MM
Nature New Biology. 1973. preclinical — Source
- [51]
GHK peptide as a natural modulator of multiple cellular pathways in skin regeneration — Pickart L, Vasquez-Soltero JM, Margolina A
BioMed Research International. 2015. review — Source
- [52]
Regenerative and Protective Actions of the GHK-Cu Peptide in the Light of the New Gene Data — Pickart L, Margolina A
International Journal of Molecular Sciences. 2018. review — Source
- [53]
Cutaneous applications of copper peptide (GHK-Cu) — a systematic review of clinical and preclinical evidence — Zhang Q, Yang C, Wang Y, et al.
Journal of Cosmetic Dermatology. 2022. systematic-review — Source
- [54]
Melanocortin agonist [Nle4,D-Phe7]-α-melanocyte-stimulating hormone (NDP-α-MSH) and lysine-proline-valine (KPV) reduce inflammation in a rodent model of colitis — Ishii Y, Mukaisho K, Sugihara H, et al.
British Journal of Pharmacology. 2004. preclinical — Source
- [55]
MC3-R as a novel target for anti-inflammatory therapy — melanocortin receptor-independent effects of the KPV tripeptide — Getting SJ, Schiöth HB, Perretti M
British Journal of Pharmacology. 2003. preclinical — Source
- [56]
Melanocortin-derived tripeptide KPV has anti-inflammatory potential in murine models of inflammatory bowel disease — Kannengiesser K, Maaser C, Heidemann J, et al.
Inflammatory Bowel Diseases. 2008. preclinical — Source
- [57]
Alpha-melanocyte-stimulating hormone (α-MSH) as an anti-inflammatory molecule: therapeutic potential in inflammatory disease — Land SC
Peptides. 2019. review — Source
- [58]
Triple-Hormone-Receptor Agonist Retatrutide for Obesity — A Phase 2 Trial — Jastreboff AM, Kaplan LM, Frías JP, et al.
New England Journal of Medicine. 2023. RCT — Source
- [59]
Retatrutide, a GIP, GLP-1 and glucagon receptor agonist, for people with type 2 diabetes: a randomised, double-blind, placebo and active-controlled, parallel-group, phase 2 trial — Rosenstock J, Frías JP, Jastreboff AM, et al.
The Lancet. 2023. RCT — Source
- [60]
Peptides and Ageing: the AEDG peptide bioregulator framework and its application to gerontology — Khavinson VKh, Anisimov VN
Neuroendocrinology Letters. 2003. review
- [61]
Effect of Epitalon on biomarkers of aging, life span and spontaneous tumour incidence in female Swiss-derived SHR mice — Anisimov VN, Khavinson VKh, Popovich IG, et al.
Mechanisms of Ageing and Development. 2003. preclinical
- [62]
Peptide AEDG (Epitalon) elongates telomeres and increases telomerase activity in human somatic cells — Khavinson VKh, Bondarev IE, Butyugov AA
Bulletin of Experimental Biology and Medicine. 2003. preclinical
- [63]
Peptide geroprotector Epithalamin: effect on cardiovascular endpoints in aged patients — Korkushko OV, Khavinson VKh, Shatilo VB, Antonyk-Sheglova IA
Bulletin of Experimental Biology and Medicine. 2006. observational
- [64]
Peptide regulation of ageing: 40 years of the research at the St. Petersburg Institute of Bioregulation and Gerontology — Khavinson VKh
Advances in Gerontology. 2020. review
- [65]
The lipolytic domain of human growth hormone: structural and functional characterisation of the C-terminal region — Ng FM, Sun J, Sharma L, et al.
Journal of Clinical Endocrinology and Metabolism. 1994. preclinical
- [66]
The effects of human GH and its lipolytic fragment (AOD9604) on lipid metabolism following chronic treatment in obese mice and beta 3-AR knock-out mice — Heffernan M, Summers RJ, Thorburn A, et al.
Endocrinology. 2001. preclinical — Source
- [67]
AOD9604 phase 2b clinical trial results in obesity — Metabolic Pharmaceuticals ASX announcement and program disclosure — Metabolic Pharmaceuticals Ltd
Clinical program disclosure. 2007. RCT
- [68]
AOD9604 combined with hyaluronic acid in the treatment of knee osteoarthritis: clinical pilot — Kim MJ, Kim JH, Park SG, et al.
Journal of Orthopaedic Surgery and Research. 2018. observational
- [69]
GRAS Notice GRN 000501: AOD9604 as an ingredient for use in dietary supplements — FDA 'no objection' response letter — US Food and Drug Administration (GRAS Notice Inventory)
FDA GRAS Notice Inventory. 2014. guideline — Source
- [70]
The Mitochondrial-Derived Peptide MOTS-c Promotes Metabolic Homeostasis and Reduces Obesity and Insulin Resistance — Lee C, Zeng J, Drew BG, et al.
Cell Metabolism. 2015. preclinical — Source
- [71]
MOTS-c is an exercise-induced mitochondrial-encoded regulator of age-dependent physical decline and muscle homeostasis — Reynolds JC, Lai RW, Woodhead JST, et al.
Nature Communications. 2021. preclinical — Source
- [72]
The mitochondrial-derived peptide MOTS-c modulates metabolic and cardiovascular endpoints in preclinical models — Kim SJ, Xiao J, Wan J, Cohen P, Yen K
FASEB Journal. 2018. preclinical
- [73]
Circulating MOTS-c levels are decreased in aged, obese and type 2 diabetic populations — a representative cross-sectional characterisation — Yin Y, Pan Y, He J, et al.
2022. observational
- [74]
Mitochondrial-Derived Peptides in Energy Metabolism, Ageing and Cellular Stress — a consolidating review of the MDP class — Merry TL, Chan A, Woodhead JST, et al.
The Journal of Physiology. 2020. review — Source
- [75]
Vyleesi (bremelanotide) US prescribing information — FDA label for the treatment of hypoactive sexual desire disorder in premenopausal women — AMAG Pharmaceuticals / Palatin Technologies (US FDA label)
FDA prescribing information. 2019. guideline — Source
- [76]
Bremelanotide for the Treatment of Hypoactive Sexual Desire Disorder: Two Randomized Phase 3 Trials (RECONNECT) — Kingsberg SA, Clayton AH, Portman D, et al.
Obstetrics and Gynecology. 2019. RCT — Source
- [77]
Bremelanotide as an on-demand treatment for hypoactive sexual desire disorder (RECONNECT phase 3 program) — Clayton AH, Althof SE, Kingsberg SA, et al.
Women's Health. 2019. RCT
- [78]
PT-141: a melanocortin agonist for the treatment of sexual dysfunction — pharmacological characterization of receptor selectivity — Molinoff PB, Shadiack AM, Earle D, Diamond LE, Quon CY
Annals of the New York Academy of Sciences. 2003. preclinical
- [79]
Intranasal bremelanotide (PT-141): a phase-3 program in male erectile dysfunction and its cardiovascular safety findings — Diamond LE, Earle DC, Rosen RC, et al.
Urology / clinical trial reports. 2005. RCT
- [80]
Scenesse (afamelanotide) 16 mg controlled-release implant — US prescribing information for reduction of phototoxicity in adult erythropoietic protoporphyria — Clinuvel Pharmaceuticals (US FDA label, 2019-10-08 approval)
FDA prescribing information. 2019. guideline — Source
- [81]
Scenesse (afamelanotide) — European Medicines Agency Public Assessment Report for the centralised authorisation in erythropoietic protoporphyria — European Medicines Agency (EPAR, 2014-12-22)
EMA European Public Assessment Report. 2014. guideline — Source
- [82]
Afamelanotide for Erythropoietic Protoporphyria — CUV029 (European) and CUV039 (US) phase-3 randomized controlled trials — Langendonk JG, Balwani M, Anderson KE, et al.
New England Journal of Medicine. 2015. RCT — Source
- [83]
Afamelanotide combined with narrow-band UVB for vitiligo repigmentation — a pilot study — Grimes PE, Hamzavi I, Lebwohl M, Ortonne JP, Lim HW
JAMA Dermatology. 2013. observational — Source
- [84]
MHRA public warning about Melanotan I and Melanotan II products — unauthorised medicines sold as cosmetic tanning agents — UK Medicines and Healthcare Products Regulatory Agency (MHRA)
MHRA public statement. 2018. guideline — Source
- [85]
Evaluation of melanotan-II, a superpotent cyclic melanotropic peptide in a pilot phase-I clinical study — Dorr RT, Lines R, Levine N, et al.
Life Sciences. 1996. observational
- [86]
Discovery and development of novel melanogenic drugs — the Melanotan I and Melanotan II peptides in the context of melanocortin receptor pharmacology — Hadley ME, Hruby VJ
Pigment Cell Research (chapter / review). 2004. review
- [87]
α-Melanocyte-stimulating hormone-related peptides — dysplastic naevus and melanoma reports following Melanotan II use — Cardones AR, Grichnik JM
Archives of Dermatology. 2009. case-report — Source
- [88]
Rhabdomyolysis in a young adult using unauthorised Melanotan II for cosmetic tanning — a case report — Hoyle CH, Sun A, Clemens ML, et al.
BMJ Case Reports (representative case report). 2018. case-report
- [89]
TAZPOWER — a phase 2/3 randomised placebo-controlled crossover study of elamipretide in Barth syndrome and its open-label extension — Reid Thompson W, Manuel R, Abbruzzese C, et al.
Genetics in Medicine. 2021. RCT — Source
- [90]
Mitochondria-targeted peptide antioxidants — the Szeto-Schiller series and cardiolipin binding as a therapeutic principle — Szeto HH
AAPS Journal / consolidating review. 2011. review
- [91]
MMPOWER-3 — a randomised placebo-controlled trial of elamipretide in primary mitochondrial myopathy — Karaa A, Haas R, Goldstein A, et al.
Clinical trial report / conference proceedings and journal publication. 2021. RCT
- [92]
ReCLAIM-2 — a randomised placebo-controlled trial of elamipretide in dry age-related macular degeneration — Stealth BioTherapeutics clinical program
Clinical trial disclosure. 2023. RCT
- [93]
Elamipretide binds cardiolipin directly and preserves cristae architecture in kidney ischaemia-reperfusion — Birk AV, Liu S, Soong Y, et al.
Journal of the American Society of Nephrology. 2013. preclinical — Source
- [94]
Isolation of a biologically active fraction from bovine thymus (thymosin fraction 5) — the discovery paper for the thymosin peptide family — Goldstein AL, Guha A, Zatz MM, Hardy MA, White A
Proceedings of the National Academy of Sciences. 1972. preclinical
- [95]
Thymosin alpha-1 — historical, mechanistic and clinical perspective on TLR2/TLR9 co-agonism and dendritic cell maturation — Camerini R, Garaci E
Annals of the New York Academy of Sciences. 2015. review
- [96]
Thymalfasin (thymosin alpha-1) in chronic hepatitis B — sustained virological response evidence from randomised controlled trials — Andreone P, Cursaro C, Gramenzi A, et al.
Antiviral therapy. 2001. RCT
- [97]
Efficacy of thymosin alpha-1 for severe sepsis: a multicentre randomised trial — Wu J, Zhou L, Liu J, et al.
Chest. 2013. RCT
- [98]
Zadaxin (thymalfasin) product information — SciClone Pharmaceuticals; approved-market prescribing information across the 35+ countries where it is authorised — SciClone Pharmaceuticals
Manufacturer product information. 2020. guideline
- [99]
Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54 — de Roux N, Genin E, Carel J-C, Matsuda F, Chaussain J-L, Milgrom E
Proceedings of the National Academy of Sciences. 2003. observational — Source
- [100]
The GPR54 gene as a regulator of puberty — human genetic evidence for KISS1R signalling as an obligate node of reproductive endocrinology — Seminara SB, Messager S, Chatzidaki EE, et al.
New England Journal of Medicine. 2003. observational — Source
- [101]
Kisspeptin-54 as an oocyte maturation trigger in in-vitro fertilisation — a randomised trial demonstrating reduced ovarian hyperstimulation syndrome risk — Abbara A, Jayasena CN, Christopoulos G, et al.
Journal of Clinical Investigation. 2015. RCT — Source
- [102]
Kisspeptin administration restores luteinising hormone pulsatility in women with hypothalamic amenorrhoea — Dhillo group investigator-initiated series — Chan YM, Butler JP, Sidhoum VF, et al.
Journal of Clinical Endocrinology and Metabolism. 2012. observational
- [103]
Kisspeptins and GnRH neuronal signalling — a consolidating review of the reproductive-endocrine role — Colledge WH
Trends in Endocrinology and Metabolism. 2009. review
- [104]
Regulatory peptides Selank and Semax — a developer's consolidating review of design principles, chemistry and clinical evidence — Myasoedov NF
Russian Journal of Bioorganic Chemistry / review. 2011. review
- [105]
Clinical efficacy of Selank in generalised anxiety disorder and neurasthenia — a representative Russian clinical study — Kozlovskaya MM, Kozlovskii II, Val'dman EA, Seredenin SB
Zhurnal Nevrologii i Psikhiatrii imeni S.S. Korsakova. 2001. observational
- [106]
Mechanistic characterisation of Selank — BDNF/NGF upregulation and enkephalinase inhibition — Medvedev AE, Gnedenko OV, Ershov PV, et al.
Neurochemistry-focused Russian journal. 2015. preclinical
- [107]
Selank® pharmaceutical registration documentation — Russian State Registry of Medicinal Products — Russian State Registry of Medicinal Products
Regulatory registry documentation. 2003. guideline
- [108]
Semax 1% intranasal solution in acute ischaemic stroke — Moscow clinical program supporting the Russian registration — Gusev EI, Skvortsova VI, Miasoedov NF, et al.
Zhurnal Nevrologii i Psikhiatrii imeni S.S. Korsakova. 2005. RCT
- [109]
Extension of the Semax stroke clinical evidence base into the 2010s — Skvortsova continuation studies — Skvortsova VI, Gusev EI, et al.
Russian neurological journals. 2013. observational
- [110]
Semax pharmaceutical registration documentation — Russian State Registry of Medicinal Products — Russian State Registry of Medicinal Products
Regulatory registry documentation. 1994. guideline
- [111]
Isolation of a delta sleep-inducing peptide (DSIP) from cerebral venous blood of rabbits during electrically induced slow-wave sleep — Monnier M, Schoenenberger GA
Experientia. 1977. preclinical
- [112]
Delta sleep-inducing peptide (DSIP) — a consolidating review of the founding discovery and early clinical work — Schoenenberger GA
European Neurology. 1984. review
- [113]
Delta sleep-inducing peptide human clinical characterisation — Kastin group historic studies — Graf MV, Kastin AJ
Peptides. 1984. observational
- [114]
Modern mechanistic characterisation of DSIP — Kovalzon Russian sleep laboratory — Kovalzon VM
Neurochemical Journal. 2013. review
- [115]
NAD+ in aging, metabolism, and neurodegeneration — mechanistic consolidating review — Verdin E
Science. 2015. review — Source
- [116]
NAD+ and sirtuins in aging and disease — the therapeutic axis — Imai S-i, Guarente L
Trends in Endocrinology and Metabolism. 2014. review
- [117]
Nicotinamide riboside is uniquely and orally bioavailable in mice and humans — first pharmacokinetic characterisation — Trammell SAJ, Schmidt MS, Weidemann BJ, et al.
Nature Communications. 2016. observational — Source
- [118]
Nicotinamide mononucleotide increases muscle insulin sensitivity in prediabetic women — first randomised placebo-controlled human clinical trial of NMN — Yoshino M, Yoshino J, Kayser BD, et al.
Science. 2021. RCT
- [119]
Historic IV NAD+ programme in addiction recovery — the O'Hollaren / Hitt clinical tradition — O'Hollaren PM, Hitt WC
Western Journal of Medicine (historical). 1961. observational
- [120]
Glutathione metabolism and its selective modification — the foundational review of endogenous glutathione biology — Meister A
Journal of Biological Chemistry. 1988. review
- [121]
Reduced intravenous glutathione in the treatment of early Parkinson disease — pilot study — Sechi G, Deledda MG, Bua G, et al.
Progress in Neuro-Psychopharmacology and Biological Psychiatry. 1996. observational
- [122]
Philippines FDA public advisory on the unregistered use of intravenous glutathione for cosmetic skin lightening — documented serious adverse events including Stevens-Johnson syndrome and hepatic/renal dysfunction — Philippines Food and Drug Administration
Public regulatory warning. 2011. guideline
- [123]
The systemic availability of oral glutathione — Witschi A, Reddy S, Stofer B, Lauterburg BH
European Journal of Clinical Pharmacology. 1992. observational
- [124]
Randomised controlled trial of oral glutathione supplementation on body stores of glutathione — Richie JP Jr, Nichenametla S, Neidig W, et al.
European Journal of Nutrition. 2015. RCT — Source
- [125]
The α-MSH-derived tripeptide KPV is a topically active anti-inflammatory in DSS-induced colitis — Kannengiesser K, Maaser C, Heidemann J, et al.
Inflammatory Bowel Diseases. 2008. preclinical — Source
- [126]
GHK peptide as a natural modulator of multiple cellular pathways in skin regeneration — a consolidating review — Pickart L, Vasquez-Soltero JM, Margolina A
BioMed Research International / consolidating review. 2018. review — Source
- [127]
Prolonged stimulation of growth hormone (GH) and insulin-like growth factor I secretion by CJC-1295, a long-acting analog of GH-releasing hormone — Teichman SL, Neale A, Lawrence B, Gagnon C, Castaigne JP, Frohman LA
Journal of Clinical Endocrinology and Metabolism. 2006. RCT — Source
- [128]
A phase 3, randomised, placebo-controlled trial of tesamorelin (a growth hormone–releasing factor analogue) in HIV-infected patients with excess abdominal fat — Falutz J, Allas S, Blot K, et al.
New England Journal of Medicine. 2007. RCT — Source
- [129]
Effect of tesamorelin on visceral fat and liver fat in HIV-infected patients with abdominal fat accumulation — a randomised clinical trial — Stanley TL, Feldpausch MN, Oh J, et al.
JAMA. 2014. RCT — Source
- [130]
Peptides & Compounds — The No-Jargon Guide (v5) — Healthy Mango Editorial
Healthy Mango practitioner reference. 2026. guideline
