RE:RE:RE:RE:RE:RE:RE:RE:RE:National Bank On ThRight but I don't think anyone really believes that to be a real issue after all these years of Egrifta use without the drug being pulled from the market for causing cancer. If people really believed the risk factors listed on the FDA info for most drugs, they might never take any drug.
PWIB123 wrote: Increased risk of cancer is still listed as one of the potential negative side effects on the website. https://www.egriftasv.com/en/
SPCEO1 wrote: That was from way back - it came up during the FDA Advocacy hearing for Egrifta. I don't think it has been a concern ever since and I have never seen any data that suggests it is a problem.
palinc2000 wrote: Increased risks of cancer??
As you know I am not a scientist ....Where did you see that?
PWIB123 wrote: If I remember correctly, some of the ideas expressed on why THTX would still have a viable marketplace for NASH are as follows:
1. Tesamorelin sold as EGRIFTA is already a commercialized HIV drug and could be dual labeled. Seems to reason HIV patients would change their drug regiment to include EGRIFTA to also combat NASH instead of adding another drug to their regiment.
2. Not everyone enjoys taking pills and would choose a different option if the circumstances made sense.
3. Combination therapies can enhance drug regiments and Tesamorelin may be better for the patient based on the other drugs they're already taking. This would be especially true if EGRIFTA turns out to have all the additional benefits that are also being studied.
4. Pretty sure there was data around adherance to the patients plan.
Ironically, one ofthe side effects of EGRIFTA is an increased risk of a new cancer or reactivation of a past cancer coming back.
Trogarzon wrote: Onthe Nash renewd interest I agree but Madrigal (MDGL) met both endpoints in P3 with flying colors.. like 60%+ improvement vs like 38% for THTX on top of Fibrosis improvements. Even if TH has a path forward why would they approve it when the bar has been set so hight by Madrigal.