Does anyone know why the clinical trials for enclomiphene ended prematurely?
Was it because of low participant satisfaction or some other reason?
Was it because of low participant satisfaction or some other reason?
The FDA banned enclomiphene.Does anyone know why the clinical trials for enclomiphene ended prematurely?
Was it because of low participant satisfaction or some other reason?
I believe this was the final nail in the coffin. Repros perhaps sensed moving goalposts and couldn't risk additional expenditures.Does anyone know why the clinical trials for enclomiphene ended prematurely?
Was it because of low participant satisfaction or some other reason?
Thank you Dear Heavenly Father/Mother/Other for our beloved Cataceous.I believe this was the final nail in the coffin. Repros perhaps sensed moving goalposts and couldn't risk additional expenditures.
In the letter, the FDA stated that, based on recent scientific developments, the design of enclomiphene Phase 3 studies is no longer adequate to demonstrate clinical benefit and recommended that Repros conduct an additional Phase 3 study or studies to support approval in the target population. The FDA also noted concerns regarding study entry criteria, titration and bioanalytical method validation in the Phase 3 program.
More recently the FDA declined to add enclomiphene to the 503A Bulks List, which in time will make pharmaceutical-grade enclomiphene unavailable in the U.S. I can't vouch for its accuracy, but a couple months ago an online source claimed that the Bulks List had not been updated yet, allowing a temporary stay of execution.
Thanks, Cat.I believe this was the final nail in the coffin. Repros perhaps sensed moving goalposts and couldn't risk additional expenditures.
In the letter, the FDA stated that, based on recent scientific developments, the design of enclomiphene Phase 3 studies is no longer adequate to demonstrate clinical benefit and recommended that Repros conduct an additional Phase 3 study or studies to support approval in the target population. The FDA also noted concerns regarding study entry criteria, titration and bioanalytical method validation in the Phase 3 program.
More recently the FDA declined to add enclomiphene to the 503A Bulks List, which in time will make pharmaceutical-grade enclomiphene unavailable in the U.S. I can't vouch for its accuracy, but a couple months ago an online source claimed that the Bulks List had not been updated yet, allowing a temporary stay of execution.
I think there are two possibilities:Thanks, Cat.
Do you know why most guys feel pretty much the same in all areas when taking enclomiphene, even when testosterone can raise by more than 3 times baseline?
Does anyone know why the clinical trials for enclomiphene ended prematurely?
Was it because of low participant satisfaction or some other reason?
When taking enclomiphene, my estraiol was 50% above the reference range and DHT had doubled from baseline levels. Despite that, I noticed no increase in libido, no increase in muscle strength, no increase in energy level or improvement in mood.I think there are two possibilities:
1) Testosterone is just a prohormone for DHT and estradiol in most tissues and is relatively inert by itself, with some exceptions like anabolic effects in muscle. Blocking estrogen receptors with estradiol may block many of the benefits of higher testosterone which are mediated by conversion to estradiol. This is especially relevant in the brain.
2) In some guys (many guys?), there is just not that much subjective difference between low normal and high normal testosterone levels. I wouldn't have believed this before spending a few months on TRT myself. Some percentage of men underwhelmed by enclomiphene will also be underwhelmed by TRT for this reason.
Clomid and enclomiphene blocks neurotransmitter estrogen receptors, blocks receptors in the heart, liver and the pancreas.Also when I tried hCG monotherapy, it did not bring my T level up as high as clomid and enclomiphene did, but energy and libido were much higher.
Possibly because with Clomid you're counteracting the reduction in estrogenic activity caused by enclomiphene; the zuclomiphene isomer of Clomid acts as an estrogen. It's been suggested that serum estradiol measurements have less value when one is using a SERM—they're not accurately reflecting overall estrogenic activity, and they can't tell you anything about shifts in relative estrogenic activity between various sites.When taking enclomiphene, my estraiol was 50% above the reference range and DHT had doubled from baseline levels. Despite that, I noticed no increase in libido, no increase in muscle strength, no increase in energy level or improvement in mood.
What I did notice was that the skin on my face became a lot more oily and my appetite increased, which resulted in an 8lb weight gain over 2 months.
When I took regular clomid, I noticed a significant increase in libido and muscle strength over the first month before the negative side effects kicked in.
Why would this occur from clomid but not enclomiphene?
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Increased testosterone with estrogen receptor blockade = benefit blockade in many people.When taking enclomiphene, my estradiol was 50% above the reference range and DHT had doubled from baseline levels. Despite that, I noticed no increase in libido, no increase in muscle strength, no increase in energy level or improvement in mood.
You still had plenty of AR agonism despite the ER shenanigans.What I did notice was that the skin on my face became a lot more oily
ER agonism of zuclomiphene might have countered the ER antagonism of enclomiphene for awhile and allowed some beneficial effects to sneak through.When I took regular clomid, I noticed a significant increase in libido and muscle strength over the first month before the negative side effects kicked in.
Why would this occur from clomid but not enclomiphene?
Increased testosterone with unblocked estrogen receptors = benefits realized.Also when I tried hCG monotherapy, it did not bring my T level up as high as clomid and enclomiphene did, but energy and libido were much higher.
I think you're probably right!Possibly because with Clomid you're counteracting the reduction in estrogenic activity caused by enclomiphene; the zuclomiphene isomer of Clomid acts as an estrogen. It's been suggested that serum estradiol measurements have less value when one is using a SERM—they're not accurately reflecting overall estrogenic activity, and they can't tell you anything about shifts in relative estrogenic activity between various sites.
Thanks. I think that's an accurate assessment of what occurred.Here are my interpretations of your experience:
Increased testosterone with estrogen receptor blockade = benefit blockade in many people.
You still had plenty of AR agonism despite the ER shenanigans.
ER agonism of zuclomiphene might have countered the ER antagonism of enclomiphene for awhile and allowed some beneficial effects to sneak through.
Increased testosterone with unblocked estrogen receptors = benefits realized.
The usual benefits of testosterone on muscle strength and growth will be at least partially countered by enclomiphene's reduction of IGF-1. Estradiol also has anabolic effects in both muscle and connective tissue. I think Enclomiphene could cause the joint soreness associated with low estradiol by blocking estrogen receptors in the joints.Just wondering why the AR agonism that caused the oily skin did not also result in greater muscle strength? I thought that elevation in DHT normally increases muscle strength?
One other side effect I got from enclomiphene was that my muscles and joints felt a bit more sore than usual even though I did not make any changes to my exercise routine. Could this be because enclomiphene blocks estrogen receptors in the muscles too?
I don't agree that the "sensitive" test is necessarily the correct one. For me it has been highly problematic, such that I rely exclusively on the regular immunoassay test. However, the standard test can have significant cross-reactivities, so you have to be confident that these don't apply to your situation before relying on it....
Btw the serum estradiol test was just the regular estradiol test, not the sensitive estradiol test.
Could you please explain why the sensitive estradiol test is the correct one that men should use?
Dr. Crisler mentioned many times, you cannot assay estrogen properly whilst taking a SERM.Possibly because with Clomid you're counteracting the reduction in estrogenic activity caused by enclomiphene; the zuclomiphene isomer of Clomid acts as an estrogen. It's been suggested that serum estradiol measurements have less value when one is using a SERM—they're not accurately reflecting overall estrogenic activity, and they can't tell you anything about shifts in relative estrogenic activity between various sites.