Ostarine clinical trials

user567

Active member
Awards
3
  • Established
  • First Up Vote
  • Best Answer
A lot of people think Ostarine is just a "research chemical" at this point but the fact is this drug has been well studied for years in clinical trials. Over 1700 patients in doses from .1 to 100mg! The latest is a phase II study to treat incontinence in women. Interestingly it works by strengthening the muscles controlling the bladder. More info below but studies are showing this is a safe well tolerated drug. The study below was woman taking 3mg daily.


The proof-of-concept phase II study was initiated in the first quarter of 2016. In this study, enobosarm is administered to post-menopausal women who have showed SUI symptoms for more than six months.

The study revealed that women treated with enobosarm lead to a significant reduction in incontinence episodes per day with decrease in mean stress leaks by over 80% from baseline across 12 weeks. Adverse events reported in the study are minimal.
 
Nac

Nac

Well-known member
Awards
3
  • Established
  • First Up Vote
  • RockStar
Strange, I have a 2016 interview with Dalton saying ostarine has been scrapped as an investigational drug.
 
Smont

Smont

Legend
Awards
5
  • Established
  • First Up Vote
  • Best Answer
  • RockStar
  • Legend!
Strange, I have a 2016 interview with Dalton saying ostarine has been scrapped as an investigational drug.
They been gave up on it unless I missed something
 
Nac

Nac

Well-known member
Awards
3
  • Established
  • First Up Vote
  • RockStar
The enobosarm saga

Enobosarm is a drug that, by all accounts, builds muscle mass and strength with acceptable side effects. Yet it failed because of regulatory constraints that all companies in the atrophy space must confront.

Discovered and developed by the Memphis, Tennessee–based biotech company GTx, enobosarm, as a SARM, binds the androgen receptor like testosterone but with tissue selectivity. Enobosarm lacks testosterone's steroid rings and thus cannot convert to dihydrotestosterone, which promotes prostate growth (and cancer). Another advantage is it doesn't have testosterone's masculinizing side effects in women, nor can it be converted by aromatases to estrogen. Its effects are largely confined to muscle, and it works; SARMs “will at relatively high doses increase muscle strength,” says St. Louis University geriatrician John Morley. “I don't think there's any real question.”

In a phase 2 trial of testing individuals with sarcopenia, GTx reported a 3% increase in lean body mass and a 15% boost in muscle stair-climbing power11. Enobosarm was well-tolerated, although it lowered serum high-density lipoprotein. So to advance the drug further in sarcopenia, the FDA required a cardiovascular safety study, which GTx estimated would cost $500 million, well beyond its means. “You have to do some really big cardiovascular safety studies if you're going into an otherwise healthy population like frail men and women,” says James Dalton, GTx's former CSO. The company scrapped plans for phase 3 in sarcopenia and chose to test enobosarm in cancer cachexia instead, where the FDA was less concerned about long-term heart effects.

In phase 3 testing, enobosarm boosted lean muscle mass in two separate trials, but stair-climbing power only in one, and only relative to placebo (i.e., no absolute increase was demonstrated). That could have been enough for approval in Europe, but not in the US, where the FDA wanted to see strength grow. That's something very hard to show in declining cancer patients undergoing aggressive therapy, says Dalton, now dean of pharmaceutical sciences at the University of Michigan. GTx decided not to file, giving up on enobosarm for treating muscle disorders. “A business and regulatory decision, more than anything else,” says Dalton, who is convinced that enobosarm is safe and effective at building and strengthening muscle. “I would take the drug today,” he says. Many people do. Illegal sales of enobosarm, also known as ostarine, are rampant on the internet.

Cancer cachexia was a problematic indication, in Morley's view, because the severity of the background illness muddied enobosarm's positive effects on muscle. Enobosarm “did wonderfully well when it was tested in old people,” he says. “Really as good as anybody's seen, both for building muscle and strength in a short period of time.” Dalton's one regret is that GTx didn't test a higher dose that would have overcome the negative effects of cancer and proven to the FDA's satisfaction that enobosarm works.

http://www.nature.com/nbt/journal/v34/n5/box/nbt.3557_BX2.html?foxtrotcallback=true
 
dezzy84

dezzy84

Member
Awards
2
  • Established
  • First Up Vote
The enobosarm saga

Enobosarm is a drug that, by all accounts, builds muscle mass and strength with acceptable side effects. Yet it failed because of regulatory constraints that all companies in the atrophy space must confront.

Discovered and developed by the Memphis, Tennessee–based biotech company GTx, enobosarm, as a SARM, binds the androgen receptor like testosterone but with tissue selectivity. Enobosarm lacks testosterone's steroid rings and thus cannot convert to dihydrotestosterone, which promotes prostate growth (and cancer). Another advantage is it doesn't have testosterone's masculinizing side effects in women, nor can it be converted by aromatases to estrogen. Its effects are largely confined to muscle, and it works; SARMs “will at relatively high doses increase muscle strength,” says St. Louis University geriatrician John Morley. “I don't think there's any real question.”

In a phase 2 trial of testing individuals with sarcopenia, GTx reported a 3% increase in lean body mass and a 15% boost in muscle stair-climbing power11. Enobosarm was well-tolerated, although it lowered serum high-density lipoprotein. So to advance the drug further in sarcopenia, the FDA required a cardiovascular safety study, which GTx estimated would cost $500 million, well beyond its means. “You have to do some really big cardiovascular safety studies if you're going into an otherwise healthy population like frail men and women,” says James Dalton, GTx's former CSO. The company scrapped plans for phase 3 in sarcopenia and chose to test enobosarm in cancer cachexia instead, where the FDA was less concerned about long-term heart effects.

In phase 3 testing, enobosarm boosted lean muscle mass in two separate trials, but stair-climbing power only in one, and only relative to placebo (i.e., no absolute increase was demonstrated). That could have been enough for approval in Europe, but not in the US, where the FDA wanted to see strength grow. That's something very hard to show in declining cancer patients undergoing aggressive therapy, says Dalton, now dean of pharmaceutical sciences at the University of Michigan. GTx decided not to file, giving up on enobosarm for treating muscle disorders. “A business and regulatory decision, more than anything else,” says Dalton, who is convinced that enobosarm is safe and effective at building and strengthening muscle. “I would take the drug today,” he says. Many people do. Illegal sales of enobosarm, also known as ostarine, are rampant on the internet.

Cancer cachexia was a problematic indication, in Morley's view, because the severity of the background illness muddied enobosarm's positive effects on muscle. Enobosarm “did wonderfully well when it was tested in old people,” he says. “Really as good as anybody's seen, both for building muscle and strength in a short period of time.” Dalton's one regret is that GTx didn't test a higher dose that would have overcome the negative effects of cancer and proven to the FDA's satisfaction that enobosarm works.

http://www.nature.com/nbt/journal/v34/n5/box/nbt.3557_BX2.html?foxtrotcallback=true
So they are scrapping it then?
 
Nac

Nac

Well-known member
Awards
3
  • Established
  • First Up Vote
  • RockStar
Dalton didnt come right out and specifically say "ostarine is being scrapped" but his comments seem to indicate it has a limited future at best (as a pharma FDA approved drug).
 

mike33511

Well-known member
Awards
1
  • Established
There is a reason it was only studied on post-menopausal women. I would never let a woman I cared about touch Ostarine if there was a chance she might want to have a child in the future.
 
Monte Brogan

Monte Brogan

Member
Awards
1
  • Established
Nac, thanks for posting this interesting article. Also highlights the immense time and cost required to bring a new drug to market. Half a billion dollars for the cardiovascular trial for the sarcopenia indication - wow.

Seems like a worthwhile drug at the right dose. Hope it is eventually commercialized.
 
Monte Brogan

Monte Brogan

Member
Awards
1
  • Established
A lot of people think Ostarine is just a "research chemical" at this point but the fact is this drug has been well studied for years in clinical trials. Over 1700 patients in doses from .1 to 100mg! The latest is a phase II study to treat incontinence in women. Interestingly it works by strengthening the muscles controlling the bladder. More info below but studies are showing this is a safe well tolerated drug. The study below was woman taking 3mg daily.


The proof-of-concept phase II study was initiated in the first quarter of 2016. In this study, enobosarm is administered to post-menopausal women who have showed SUI symptoms for more than six months.

The study revealed that women treated with enobosarm lead to a significant reduction in incontinence episodes per day with decrease in mean stress leaks by over 80% from baseline across 12 weeks. Adverse events reported in the study are minimal.
Thanks for posting this. Do you have a link to the incontinence clinical trial?
 

Similar threads


Top