LEARN HOW MALEGENIX CAN GIVE YOU THE ERECTIONS YOU WANT
*Individual Results May Vary
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MALEGENIX’S REVOLUTIONARY B.A.S.E. TECHNOLOGY bridges the gap between nutrition and natural erectile process to deliver never-before-seen male enhancement results. MaleGenix utilizes time-tested solutions, optimized with modern technology, and synergized with your body’s natural processes to provide you with a longer, thicker, and harder erections every single time.
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HOW BIG CAN YOUR ERECTIONS GET? A man’s peak penis erection size is when the penile chambers are stretched to its limit, revealing the biggest that it can get naturally. Studies suggest that your peak penis erection size is dictated by a number of factors, including age, race, lifestyle choices, diet, and many more. With MaleGenix, your peak erection size can be easily achieved through a daily intake of MaleGenix, and nothing more.
BE A MALEGENIX MAN. MaleGenix Men know how it feels to be the subject of a woman’s burning lust. Experience being the object of a woman’s desire by taking MaleGenix daily!
*Individual Results May Vary
Each of the ingredients in MaleGenix has been scientifically researched to authenticate its effectiveness in erection enlargement and sexual performance.
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Get optimum testosterone boost that would maximize your libido and sexual endurance.
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Every man knows how important penis erection size is. Size definitely matters – and it’s not just with sex. A man’s penis erection size directly affects his confidence. Men with large penises erections have no problems with their sexual confidence. Their experience with women taught them that they have the upper hand in sex. Women want them – and they want them bad. It’s an exceptional experience to be wanted and be the object of a woman’s lust, and that’s why size matters for men. Having a big penis erection gives you both a physical and psychological advantage to live out your craziest sexual fantasies. With the SCIENCE OF SIZE, you now have a REAL solution that would grant you with the large erection you’ve always wanted to have. Think about it – every fantasy you’ve ever had can be yours, with just a dose of MaleGenix a day.
MaleGenix’s B.A.S.E. TECHNOLOGY is a strategy that allows top-quality male enhancement ingredients to synergize with the body’s natural process in achieving an erection, to help improve erection size. Through the B.A.S.E. TECHNOLOGY, blood volume and pressure to the cavernous spaces in the penis would be increased, forcing the elastic penile tissue to expand and create bigger erections.
MaleGenix can help you achieve the biggest erections that you could ever have by enhancing blood flow and hormone response. By taking MaleGenix consistently, you can achieve your peak length and girth.
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*Individual Results May Vary
MaleGenix is backed by more than 60 pages of scientific facts that prove its effectiveness as a comprehensive male enhancement solution. It is only fitting for us to back MaleGenix with the same confidence that the scientific researchers put into it. We have covered every purchase of MaleGenix on our official website with an ironclad 100% money back guarantee to help you make a confident purchasing decision. We have outlined several points of our product’s benefit to show you what you can expect from MaleGenix.
*Individual Results May Vary
We are 100% certain that MaleGenix will meet your expectations and amaze you with all of its benefits for sexual health. In the unlikely scenario that you are not completely satisfied with MaleGenix, you can reach out to our professional customer care representatives to assist you with refund processing. Our 100% money back guarantee entitles you to a full refund on your purchase. Through the years, we’ve only had to process refunds on a number of occasions. Rest assured, our refunds & return processes would be short, swift, and stress-free.
MaleGenix covers all purchases originating from our official website with an ironclad 100% money back guarantee. In the unlikely scenario that MaleGenix failed to meet your expectations, you can reach out to us within 90 days of your purchase to process a full refund. MaleGenix has processed thousands of orders from customers, and we are proud to say that we have fulfilled every order the best way possible. We look forward to having you as our MaleGenix customer.
Treatment of erectile dysfunction often requires combinations of psychogenic and medical therapies, many of which have been only moderately successful in the past. The advent of oral phosphodiesterase type 5 (PDE-5) inhibitors, however, has greatly enhanced erectile dysfunction treatment; patients have demonstrated high tolerability and success rates for improved erectile function. The efficacy of the PDE-5 inhibitors also serves to illustrate the importance of the NO-cGMP pathway in erectile function since these agents counteract the degradation of NO-generated cGMP. Because not all patients respond to PDE-5 inhibitors, additional therapies are being investigated, such as soluble guanylyl cyclase activators and NO donors, which act on NO-independent and NO-dependent pathways, respectively.
9-HC-6-one relaxed significantly phenylephrine (PE)-precontracted CC. Such response was not attenuated by endothelium disruption, N(G) -nitro-L-arginine methyl ester, or 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one treatment, suggesting that a nitric oxide/cyclic guanosine monophosphate-dependent pathway was precluded. 9-HC-6-one attenuated PE-induced contraction by blocking cell surface and internal calcium channels with a higher potency for internal calcium release. This compound also antagonized calcium-evoked contraction in Ca2+ -free, high K+ -depolarizing condition, suggesting that interfering with the entry of calcium through voltage-dependent channels also contributed to 9-HC-6-one-induced corporal relaxation. After IC application of 9-HC-6-one, a significant rise in ICP was observed as compared with the application of normal saline. 9-HC-6-one relaxed significantly norepinephrine (NE)- and KCl-precontracted SV, and antagonized NE-induced oscillatory contraction as potent as clomipramine. Finally, the HNS-evoked increase in ILP was dose-dependently repressed after challenge by 9-HC-6-one.
Both Maca- and placebo-treated subjects experienced a significant improvement in psychological performance-related SAT-P score, but the Maca group higher than that of placebo group (+9 +/- 6 versus +6 +/- 5, P < 0.05). However, only Maca-treated patients experienced a significant improvement in physical and social performance-related SAT-P score compared with the baseline (+7 +/- 6 and +7 +/- 6, both P < 0.05). In conclusion, our data support a small but significant effect of Maca supplementation on subjective perception of general and sexual well-being in adult patients with mild ED.
Logistic regression analysis showed that Maca has an independent effect on sexual desire at 8 and 12 weeks of treatment, and this effect is not because of changes in either Hamilton scores for depression or anxiety or serum testosterone and oestradiol levels. In conclusion, treatment with Maca improved sexual desire.
The primary outcome measures were percentage changes in the Pratyatmaka Lakshanas (cardinal symptoms) of Kshina Shukra, Agni bala, Deha bala, Satva bala, the semenogram, and in the Quality of the Sexual Health Questionnaire. The placebo granules showed 70.95% improvement, whereas, the Gokshura granules showed 78.11% improvement in Rogi bala (Agni bala, Deha bala, Satva bala, and the Quality of Sexual Health) and Rogabala (Semen Analysis and Pratyatmaka Lakshanas). The Gokshura granules have shown superior results in the management of Kshina Shukra, as compared to the placebo granules.
ICA demonstrated significantly higher ICP/MAP and AUC/MAP ratios compared with control and single-dose ICA animals. Immunohistochemistry and Western blot were revealing of significantly greater positivity for nNOS and calponin in penile tissues of all test subjects treated with ICA. ICA led to significantly greater neurite length in cultured specimens of pelvic ganglia.
ICA demonstrated significantly higher ICP/MAP and AUC/MAP ratios compared with control and single-dose ICA animals. Immunohistochemistry and Western blot were revealing of significantly greater positivity for nNOS and calponin in penile tissues of all test subjects treated with ICA. ICA led to significantly greater neurite length in cultured specimens of pelvic ganglia.