Thursday, September 26, 2019 12:12:16 PM
Several points I'd make;
The price of the stock today shows market sentiment. It *seems* that there may be other compounds that are effective w/ fewer sides.
OTOH, I would argue that many of the players, like as was true in HCV, are still trying to sort NASH out. I still consider ENTA as having a fair amount of expertise in this area.
Given that..... I'm a little confused at Luly's response that the 2.5mg dose (or future undisclosed higher and lower dose, whatever they may be). It would seem that the community response it that the 2.5 dose is toast. Luly's response makes me feel ENTA hasn't discarded that. This leads me to feel that they still see it as potentially viable. I can't tell (from only having listened to it once) that they strongly favor one dose over the other. My thinking the 2.5 discontinuation rate makes it a non-player.
I harken back to viekira. What if ENTA had thrown in the towel after "failing" with that?
There seems like a disconnect in ENTA's response and the markets.
"I have not failed. I've just found 10,000 ways that won't work." Thos Edison
I'm not sure that ENTA is quite done with NASH (or FXR). I'm sure that several other companies probably are.
It is certainly true that both intercept and Gilead seemed positive with their results and the market was also very underwhelmed. My thinking is that the pros are less crushed by "failure" than the market. I have no clue. I only see the failure. Luly, ENTA and others who have expertise see the ares in which they succeeded and want to continue going to the next step.
The ultimate winner won't be the company that fails and quits. That may be the preferred course that many would take today. Fewer still are those who get it right on the first try.
The price of the stock today shows market sentiment. It *seems* that there may be other compounds that are effective w/ fewer sides.
OTOH, I would argue that many of the players, like as was true in HCV, are still trying to sort NASH out. I still consider ENTA as having a fair amount of expertise in this area.
Given that..... I'm a little confused at Luly's response that the 2.5mg dose (or future undisclosed higher and lower dose, whatever they may be). It would seem that the community response it that the 2.5 dose is toast. Luly's response makes me feel ENTA hasn't discarded that. This leads me to feel that they still see it as potentially viable. I can't tell (from only having listened to it once) that they strongly favor one dose over the other. My thinking the 2.5 discontinuation rate makes it a non-player.
I harken back to viekira. What if ENTA had thrown in the towel after "failing" with that?
There seems like a disconnect in ENTA's response and the markets.
"I have not failed. I've just found 10,000 ways that won't work." Thos Edison
I'm not sure that ENTA is quite done with NASH (or FXR). I'm sure that several other companies probably are.
It is certainly true that both intercept and Gilead seemed positive with their results and the market was also very underwhelmed. My thinking is that the pros are less crushed by "failure" than the market. I have no clue. I only see the failure. Luly, ENTA and others who have expertise see the ares in which they succeeded and want to continue going to the next step.
The ultimate winner won't be the company that fails and quits. That may be the preferred course that many would take today. Fewer still are those who get it right on the first try.
Recent ENTA News
- Form S-8 - Securities to be offered to employees in employee benefit plans • Edgar (US Regulatory) • 05/13/2026 11:25:49 AM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 05/13/2026 11:00:39 AM
- Form 8-K - Current report • Edgar (US Regulatory) • 05/11/2026 08:05:17 PM
- Enanta Pharmaceuticals Reports Financial Results for its Fiscal Second Quarter Ended March 31, 2026 • Business Wire • 05/11/2026 08:01:00 PM
- Enanta Pharmaceuticals to Present Data for its Respiratory Syncytial Virus and STAT6 Inhibitor Programs at the American Thoracic Society International Conference 2026 • Business Wire • 05/04/2026 11:00:00 AM
- Enanta Pharmaceuticals Announces First Participant Dosed in Phase 1 Clinical Trial of EDP-978, an Oral, Once-Daily KIT Inhibitor, in Development for the Treatment of Urticaria • Business Wire • 04/13/2026 11:00:00 AM
- Enanta Pharmaceuticals to Present Data for Zelicapavir, an Oral, Once-Daily, N-Protein Inhibitor, in Development for the Treatment of Respiratory Syncytial Virus, at ESCMID Global 2026 • Business Wire • 04/07/2026 11:00:00 AM
- Enanta Pharmaceuticals to Present Data for its STAT6 Inhibitor Program at IMMUNOLOGY2026TM, the Annual Meeting of the American Association of Immunologists (AAI) • Business Wire • 03/30/2026 11:00:00 AM
- Form 8-K - Current report • Edgar (US Regulatory) • 03/26/2026 12:00:07 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 03/13/2026 08:20:56 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 03/13/2026 08:18:09 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 03/13/2026 08:17:04 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 03/13/2026 08:14:14 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 03/12/2026 08:05:29 PM
- Enanta Pharmaceuticals to Present at The Citizens Life Sciences Conference • Business Wire • 03/03/2026 12:00:00 PM
- Form EFFECT - Notice of Effectiveness • Edgar (US Regulatory) • 02/23/2026 05:15:10 AM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 02/13/2026 09:33:34 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 02/13/2026 09:31:44 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 02/13/2026 09:29:51 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 02/13/2026 09:28:45 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 02/13/2026 09:27:26 PM
- Form S-3 - Registration statement under Securities Act of 1933 • Edgar (US Regulatory) • 02/11/2026 09:43:43 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 02/11/2026 09:00:44 PM
- Enanta Pharmaceuticals to Present Preclinical Data for EDP-978, its KIT Inhibitor in Development for the Treatment of Type 2 Immune Diseases, at the 2026 AAAAI Annual Meeting • Business Wire • 02/10/2026 12:00:00 PM
