2/23/98UPDATED VIVUS NEWS (this Review spans the last 15 days starting with the most recent events. Post has been reformatted, upgraded.) ( This also is a continuous re-cap; just click on previous post numbers to get older posts.) Check out our marked " NEW " items, which indicate they've been added since, our previous posting. This will help folks avoid re-reading posts
************************************************************ MISCELLANEOUS MEDICAL/INVESTMENT INFO FOR NEW VIVUS INVESTORS; ============================================================= .\\\\|//// .\\ ~ ~ // .( @ @ ) ._oOOo_\_^__oOOo__ It's ok, VVUS, we all gotta be 40 someday. Yes, and even more. Frostman Oct 3 1997 : #531
================================================================= Vivus intraday chart investor.msn.com./charts/charting.asp?C2=4&Symbol=vvus ==================================================================
Last week:
2/19 Cruttenden and Roth brokered a 425,000 share trade on the downtick: Message 3476542
Zebra 12/12/97 Vivus starts primary care promotion: Message 3412899
Tunica 12/20 Better results with Axis: Message 3485422 12/12 and how to better use MUSE for better ( 70%? ) Success? Message 3414244 DRBOND 12/17 " Dynamite Vivus Review " bin Business and Medicine. Message 3455577 Message 3457556
R E F I L L CONTROVERSY: a ) 2/22:Tunica, review, Message 3502765 b ) 2/22 Frostman: Frequency of sex: Message 3498053 c ) 2/23 DRBOND Message 3502875
2/22 MissLill : thoughtful Vivus perspective: Message 3501649
2/22 TA: Viagra potential side effects research: Message 3502566
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VIVUS NEW PLANT ACTIVITY UPADATE:
Zebra update on production: Message 3377096
Tax breaks aid Vivus' incursion into Ireland -- The Business Journal of San Jose amcity.com
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VIVUS NEWSPAPERS ARTICLES :
2/6 Rubble: Feb 3, Vivus article in the GUARDIAN. Message 3356703
2/7Frostman: VIVUS 1997/1998 makes SI HOT LIST: Message 3370506
From 4 weeks ago REVIEW OF PAPERS REPORTING NBC VIVUS AD SNAFU ( gave big jolt up to Vivus ). Message 3229615
********************************************************************************************* VIVUS NEW PLANTS STATUS AND MCA /FDA APPROVAL 2/19 DR.BOND'S opinion on MCA and FDA apparoval; Message 3478490 Tax breaks aid Vivus' incursion into Ireland -- The Business Journal of San Jose amcity.com
******************************************************************************************** VIVUS MISCELLANEOUS BUSINESS Vivus announces direct to consumer campaign: Message 3209717
******************************************************************************************** VIVUS EARNINGS Mkilloran 2/10: Vivus 1999 EPS by Zacks, upgarded to $3.49 Message 3395749
******************************************************************************************** ****VIVUS JAN 15 EARNINGS CONFERENCE CALL RECAP*********
First the negatives: -Approval by the FDA will be asked by mid Feb and then we have to wait. It may be Q2 before it is inspected and approved. -Out of 1.8 mill units shipped quarterly, more than the previous Q4 150000 units are going to be shipped to Astra, at lower margins, per previous agreement. (This is something they HAVE to do; when they signed with ASTRA 1 year ago I think that they never imagined it would take this long for FDA to approve). -The above will lower margins. -Greater advertising expenses. -The decrease of Quarterly unit production from 2 mills to 1.8, due to the fact that some manpower and equipment had to be moved to new facility. -The slight decreases in demand (which I interpret as backlog decrease rather than net decrease) because of lack of advertising and lack of product availability initially. This is relative however because refills are going up. So that in absolute numbers they are still running full steam; see in next section on positives). The positives: First Mr. Wilson CEO SOUNDED MUCH MORE POSITIVE AND AGRESSIVE!!!! AND FORWARD LOOKING!!.There was NO DEFENSIVE or UNCERTAIN undertones to his voice at all that I could note. -He said at 130 mill $ sales in 97 this is one of the most successful Urology product launch ever. And this is with minimal advertising. -They will concentrate in their GIANT Ad campaign to make this the No1 and 1st prescribed drug in ED! -Giant Ad campaign to start Jan 31st with the AT&T Pebble Beach National Pro- Am Golf tournament Then ads in Newsweek Time, magazines, ABC, CBS, Wall Street Journal and other major magazines and TVs. etc. -Submit all paperwork for new factory to FDA by Feb 15 and ask them to inspect it and approve it. -They have 75 sales reps, largest in Urology. -The manufacturing problems in their new plant have been COMPLETELY corrected. -They settled their (hopefully) last lawsuit with a previous consultant, and did so to avoid prolonged litigation costs and to avoid going in front of a jury (same old reason.). The lawsuit was due apparently to a small procedural error that Vivus committed early on in their filing of the patent but which ended up costing them a lot. NOTE: without the settlement they would have made 33-cents/ share. -They have ~ 93 mill in cash: Message 3196484 -They have been accepted by all the Urologic and medical community well and Managed care so that 70% of prescriptions are now covered compared to 60% in Q2-3. -They have mailed 300,000 packages to primary care MDs across the nation, containing a sample of the MUSE system and one packet dose with aan instructional video tape about how to administer it. -They greatly stengthened management by adding to Marketing Director the previous VP of Sales of Eli Lilly. Probably one of the MOST EXCITING items is that -THEY ARE PRODUCING RIGHT N O W in the NEW PLANT, s i g n i f i c a n t amounts of product which they are STOCKPILING and which will be shipped IMMEDIATELY as soon as United Kingdom MCA approval comes. -" As for MCA plant approval, Leland did say that all data requested by the MCA to allow a FINAL APPROVAL would be submitted by mid Feb. But this date estimate IMO was a worst case scenario. VVUS could have all required data to the MCA by month end with an approval late FEB. -Also that " product at risk " will be available to be ROCKETED OUT THE DOOR, first to UK and then US as soon as approval is obtained. This could SIGNIFICANTLY IMPACT Q1 revenues if it is shipped in March to UK if MCA approves in March. Message 3197245 = MrWilson's EXACT quote (I wrote that down; everything else I am writing is out the top of my head): " You will see SIGNIFICANTLY INCREASED product NOT TOO FAR Down the road ". -They aim to be the LEADER in ED, (not 2nd to PFE, my quote, gg). He answered questions on effectiveness and demand: -Demand and acceptance have increased steadily, according to REFILL Prescription rate, which has steadily gone up, and as of Jan 3, a slow period, they are up 43% from before. -The Asensio quoted Italian study, was not published and peer reviewed, was only a letter in the Lancet, was done on the worst ED patients, they were ALL on the needle; quality of these studies was low compared to the NEJM study and their end point was not done according to established Urologic literature methods, their patients were not educated in the use of MUSE as in the NEJM study. Same would apply to the J of Urology study (less educational quality standards, but even so, in their needle patients the response was 37%, better than the 5% Italian: how do you explain that?) -The Lahey Clinic, world's most renowned diabetes center has a 50% success rate in 300 patients, same as the NEJM classic study with a 45% success rate. Lahey clinic has a much more sophisticated patient education program because they deal with diabetes. On the issue of shares sold by insiders, Wilson said that they HAVE To sell during fixed windows. That even though they sold 150000 shares in 1997, they also bought 130000. A lot was options that they exercised. As far as " share rebuying ", " and why not buy now that it's cheap ", he said that their policy is to answer that question the following quarter from the rebuy, i.e. Q2 forQ1 buys. As far as Q4 is concerned they bought ~ 300000 shares (~ $ 7.5 mill), so that they can buy 1.7 mill more that were authorized. IMHO, look for a big buy in Q1. Somebody asked about rumors of Viagra being asked for more study data by the FDA: Wilson simply stated that he would not comment to rumors. Also he did not at this cc mention of adding Viagra to MUSE like he did last time. He did not give aid and comfort to the competition guess he probably feels that Viagra must first prove itself in the medical literature and FDA before piggybacking it unto MUSE.He was also generous when the usual Zonagen question was asked: no comment (i.e. he was generous in not kicking Zonagen in the gutter where it is laying now.) In my humble opinion this was a very good cc. It answered a lot of questions. Company management came out forcefully to dispel any rumors about....gg ? Vivus demise? In Wilson's words, " While we face short term challenges...we are ready to shoot out the door with 12 cylinders, very soon ". All in my opinion only. TA *********************************************************************************************
MEDICAL ARTICLES ON VIVUS ========================== 1 )Alprostadil/Muse/Vivus Treatment of men with erectile dysfunction with transurethral alprostadil Padma Nathan H, Hellstrom WJG, Kuiser FE, Labasky, Tom Lue,Nolten,Norwood,Peterson, Shabsigh,Tam, V.Place,Gesudheit,and 90 other collaborators, for the MUSE study group. ( New England Journal of Medicine, Jan. 1997; 336: 1-7 ) Alprostadil was delivered transurethrally in a double -blind placebo-controlled study of 1511 men, 27 to 88 years of ag, who had CHRONIC erectile dysfunction.The men were first tested in the clinic with up to four doses of the drug (125,250,500,and 1000 mcg); those who had sufficient responseswere randomly assigned to treatment with either the effective dose of Alprostadil or placebo for three months at home. RESULTS ; During in- clinic testing, 996 men ( 65.9% ) had erections sufficient for intercourse.Of these men, 961 reported the results of at least one home treatment;. Of these996 men ( 65.9 % )had a erectile response satisfactory for intercourse and were subsequently entered into a placebo controlled double-blind trial: 461 received Alprostadil and 500 received placebo.Of the 461 receiving Alprostadil 299 had intercourse at least once( 64.9 % ), as compared to 93 of the 500 who received placebo ( 18.6 %, p<0.001 ) ). On average 7 of 10 men who received Alprostadil were followed by intercourse in men responsive to treatment. The efficacy of Alprostadil was similar regardless of age or the cause of erectile dysfunction, including vascular disease, diabetes, surgery and trauma ( p<0.001 for all comparisons with placebo ) . 10.8% of patients suffered from penile pain but this rarely resulted in discontinuing treatment. Hypotension occurred in the clinic in 3.3 % of men receiving Alprostadil.Hypotension- related symptoms were uncommon at home.No men had priapism or penile fibrosis. ( from the Departments of Urology of: Univ of Southern California;The Mayo Clinic ; Tulane Univ Med Center;St Louis Univ;Univ of Utah;Univ of Calif; Peachwood Medical Group,Clovis,Calif.,Univ of Wiconsin;Univ of Columbia, Columbia-Presbyterian Hospital;) ( over 100 Urologists participated in the study and are listed in the Apendix of the article). This is an important paper with large numbers of patients in a well organised study. The response rates appear surprisingly good in patients with vasculogenic impotence according to this study. ------------------------------------------------------------------- 2 )Alprostadil/Muse/Vivus after radical prostatectomy pslgroup.com ------------------------------------------------------------------- 3 )Alprostadil/Muse/ Vivus in Diabetics, one of the largest causes of impotence: vivus.com ------------------------------------------------------------------- 4 )Another study on the excellent safety of intravenous ( in the peripheral vein by drip, and then by local intracavernous injections ) of Alprostadil in the last, Oct 97 issue of ther Journal of Urology,Vol158,1403-1497; PHARMACOKINETICS OF PROSTAGLANDIN E1 AND IT'S MAINMETABOLITES AFTER INTRACAVERNOUS INJECTION AND SHORT - TERM INFUSION OF PROSTAGLANDIN E1 IN PATIENTS WITH ERECTILE DYSFUNCTION: BY Willi Cawelo,Horst Schweer, Bruno Dietrich, Hannsjofg WIlhelm, Seyberth,Albrecht et al: From the Univ of Marbufg, Ulm, Germany: www3.techstocks.com THE FUTURE!!!! Check out new study Vivus is preparing in Italy with DrGreco Ermanno: Hogher target standards than previous 2 pound study will be used ( reportedly a Lamborghini) Message 3311743 ============================================================= VIVUS COMPETITION ================= A )VIAGRA ( " THE PILL " ) by Pfizer
*NEW: PFE cut to hold because of price: Message 3399795 *NEW: HERESY: Wall Street Journal ( 2/20 ), ??DOUBTS ?? that PFE Viagra will meet sales quota? : ( needs to be confirmed, gg ). Message 3486536
-published articles ( in peer reviewed journals ): a) British Journal of Urology(1996)78, 257-261 this is the first clinical article .12 patients Message 2703575 b) International Journal of Impotence Research (1996) 8, 47-52 Message 3209803 -Zebra compares MUSE to VIAGRA Message 2817790 -phosphodiesterase ( PDE ) sideeffects ( in relation to upcoming? Approval of Viagra Sildenafil,also a PDE ):Taken from Goodman & Gillman 1996 ED.Textbook of pharmacology. www3.techstocks.com www3.techstocks.com
*NEW : *NEW: 2/22, TA : Potential Viagra side effects Message 3502566
******* B ) INVICORP ( by Senetek ),
( another needle; uses phentolamine and a so called " vasoactive peptide ". regardless, it is STILL the needle-----> pain, fibrosis, penile angulation and plaques, carrying this big shotgun in the bedroom will be a challenge in itself gg). Message 2690453 ******* C ) Harvard Scientific Liposomal sytem. ( Liposomal Delivery).
Length it takes to approve a drug: Message 3317189 2/4/98;GrandPohba critique: Message 3325245 Message 3307182 Message 3305926 Message 3307956
*NEW: Message 3315451 ********
D ) VASOMAX ( BY Zonagen )
This is generic phentolamine. No patent. Company facing multiple lawsuits for fraud. Not a contender. For details please their extensive SI post. Message 2757783 www3.techstocks.com ( PS If after you've read all of the above you are still confused, write to the Editorial Board and we'll see what we can do for you, gg, - no promises. ).
^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^ | INVESTMENT UPDATE ON VIVUS | ===========================
Vivus chart ( Brian Malloy,post #514 ). investor.msn.com./charts/charting.asp?C2=4&Symbol=vvus - Options page for VVUS: -From: Navigator One Reply #391 webservices.pcquote.com Check out Vvius 2nd opinion site;( Dr. Bond, post #207 ): etrade.stkwtch.com 2/6/98Frostman: ED PHOTO OP: Message 3363353
VIVUS PATENTS =============
Message 3316802 Message 3315857 -Vivus patent by Gene Voss, MD.- www4.techstocks.com *NEW2/20 Cacaito Vivus/HVSF patent dispute; ( note: meatus in Latin means " a hole ". HVSF has patented introduction of medication into a hole! As they say: HVSF is going down a rat hole!! GG ; TA ) Message 3491607
^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^ UNELECTED EDITORIAL BOARD
Editor Emeritus:Frostman Assistant Editor:Zebra 365, ER, M.D. Editor of sorts:Tunica Albuginea Copy Editor: Linda Kaplan Honorary Vivus Patent Holder:Gene Voss,M.D.,Cardiovasc.Anesthesia. Patent Inquiries:Whipsaw ( office unknown at this time.Possibly big city USA). Tax/IRS Dept: Zebra 365, M.D. Investment Bystanders: DR.BOND. Technical Analysis: DR.BOND,Gary Baggs Risk Analysis:David Chanin. Legal affairs,Mark Stang Vivus undercover agent, Eye Dr.Mike Vivus CPA: blankmind Still standing erect: Colby. Vivus Consulting Physicians :Edderd,David Bell,Zebra365,Cacaito, Miss Lil,Tunica Albuginea
TA |