Monday, March 24, 2008 9:24:33 AM
"From the fact that 1/3 of US women have had at least a partial hysterectomy by the time they are 60 it sounds like the medical establishment views the procedure as pretty benign"
i think it speaks more to the frequency of problems associated with uterine disease and lack of viable medical alternatives. hysterectomy is not a trivial procedure. it's certainly a bigger deal than tonsillectomy. it has more morbidity than an appendectomy. it is and should be thought of as a major abdominal procedure. an open case takes probably on average 1.5 hours, 2-3 day hospital stay, pain requiring narcotics, and a *6 week* recovery. it has a non-trivial rate of complications like wound dehiscence (just like other abdominal cases), and most gyns don't go through a career without at least one more serious complication like bladder, bowel or ureteral injury
bottom line - it's far from "benign"
"what safety the FDA will require? - directly or obliquely"
i have no idea beyond what the company has stated and has already been discussed on this board. I can add what i think the safety requirement *should* be - like any proper risk benefit assessment, the risk of the drug shoudl be weighed against the alternatives, and in this case the alternatives are invasive - so the bar should be set appropriately. adn as i have said before, the alternatives for bad endo is a life of pain, a revolving door of surgery, chronic utilization of opiates, and the bar should be somewhat different in this indication (although with this risk averse fda i doubt that will be the case)
"is it going to hit prescribing docs in the pocket book?"
good question. i'm sure there are docs that rely on surgery for a significant slice of their income, but more and more surgery is a money-losing proposition given current reimbursements. you can make mroe money per unit time in the office - in teh case of proellex endometrial monitoring with ultrasound and/or biopsy is probably a better finanical proposition at the end of the day. regardless pt demand and good practice will drive demand
i think it speaks more to the frequency of problems associated with uterine disease and lack of viable medical alternatives. hysterectomy is not a trivial procedure. it's certainly a bigger deal than tonsillectomy. it has more morbidity than an appendectomy. it is and should be thought of as a major abdominal procedure. an open case takes probably on average 1.5 hours, 2-3 day hospital stay, pain requiring narcotics, and a *6 week* recovery. it has a non-trivial rate of complications like wound dehiscence (just like other abdominal cases), and most gyns don't go through a career without at least one more serious complication like bladder, bowel or ureteral injury
bottom line - it's far from "benign"
"what safety the FDA will require? - directly or obliquely"
i have no idea beyond what the company has stated and has already been discussed on this board. I can add what i think the safety requirement *should* be - like any proper risk benefit assessment, the risk of the drug shoudl be weighed against the alternatives, and in this case the alternatives are invasive - so the bar should be set appropriately. adn as i have said before, the alternatives for bad endo is a life of pain, a revolving door of surgery, chronic utilization of opiates, and the bar should be somewhat different in this indication (although with this risk averse fda i doubt that will be the case)
"is it going to hit prescribing docs in the pocket book?"
good question. i'm sure there are docs that rely on surgery for a significant slice of their income, but more and more surgery is a money-losing proposition given current reimbursements. you can make mroe money per unit time in the office - in teh case of proellex endometrial monitoring with ultrasound and/or biopsy is probably a better finanical proposition at the end of the day. regardless pt demand and good practice will drive demand
Recent RPRX News
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 04/30/2026 09:54:06 PM
- Form 144 - Report of proposed sale of securities • Edgar (US Regulatory) • 04/28/2026 09:00:16 PM
- Royalty Pharma Launches Global Translational Prize to Recognize Breakthrough Scientific Innovation • GlobeNewswire Inc. • 04/21/2026 05:00:00 PM
- Royalty Pharma Declares Second Quarter 2026 Dividend • GlobeNewswire Inc. • 04/17/2026 12:30:00 PM
- Royalty Pharma to Announce First Quarter 2026 Financial Results on May 6, 2026 • GlobeNewswire Inc. • 04/15/2026 08:15:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 04/13/2026 01:53:04 PM
- Form ARS - Annual Report to Security Holders • Edgar (US Regulatory) • 04/10/2026 08:11:40 PM
- Form DEFA14A - Additional definitive proxy soliciting materials and Rule 14(a)(12) material • Edgar (US Regulatory) • 04/10/2026 08:11:03 PM
- Form DEF 14A - Other definitive proxy statements • Edgar (US Regulatory) • 04/10/2026 08:10:09 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 04/02/2026 09:58:57 PM
- Form 144 - Report of proposed sale of securities • Edgar (US Regulatory) • 04/01/2026 08:55:58 PM
- Royalty Pharma signs $500M co-development agreement with J&J • IH Market News • 03/30/2026 12:28:19 PM
- Royalty Pharma Announces R&D Funding Collaboration for Chronic Immune-Mediated Diseases • GlobeNewswire Inc. • 03/30/2026 11:15:00 AM
- Form 144 - Report of proposed sale of securities • Edgar (US Regulatory) • 03/23/2026 08:43:18 PM
- Royalty Pharma Appoints Lucas Glass as Head of Artificial Intelligence • GlobeNewswire Inc. • 03/23/2026 11:15:00 AM
- Form 144 - Report of proposed sale of securities • Edgar (US Regulatory) • 03/19/2026 09:12:47 PM
- Form 144 - Report of proposed sale of securities • Edgar (US Regulatory) • 03/18/2026 10:02:29 PM
- Royalty Pharma Announces Expansion of Leadership Team • GlobeNewswire Inc. • 03/17/2026 08:01:00 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 03/04/2026 10:11:47 PM
- Form 144 - Report of proposed sale of securities • Edgar (US Regulatory) • 03/04/2026 09:52:30 PM
- Form 144 - Report of proposed sale of securities • Edgar (US Regulatory) • 03/02/2026 10:26:17 PM
- Royalty Pharma Appoints Kenneth Sun as Senior Vice President and Head of Asia to Expand Royalty Pharma's Global Platform • GlobeNewswire Inc. • 03/02/2026 12:00:00 PM
- Royalty Pharma and Zymeworks Enter Into $250 Million Royalty-Backed Note Financing • GlobeNewswire Inc. • 03/02/2026 11:10:00 AM
- Zymeworks and Royalty Pharma Enter into $250 Million Royalty-Backed Note Financing • GlobeNewswire Inc. • 03/02/2026 11:01:00 AM
