InvestorsHub Logo
icon url

dav1234

02/12/14 6:08 PM

#174130 RE: biomaven0 #174129

RTRX recent uplist from OTC? Know nothing about it..pump wouldn't surprise me
icon url

dav1234

02/12/14 6:29 PM

#174132 RE: biomaven0 #174129

Retrophin Announces Agreement to Acquire Manchester Pharmaceuticals

Retrophin, Inc. (NASDAQ:RTRX)

Today : Wednesday 12 February 2014

Click Here for more Retrophin, Inc. Charts.
Acquisition Brings Two FDA-Approved Products

Management to Host Conference Call and Webcast Tomorrow at 8:30 a.m. ET

Retrophin, Inc. (NASDAQ: RTRX) today announced that it has signed an agreement to acquire Manchester Pharmaceuticals® LLC, a privately-held specialty pharmaceutical company that focuses on treatments for rare diseases. Under the terms of the agreement, Retrophin will pay a total of $62.5 million, including an upfront payment of $29.5 million, plus royalties based on product sales. The transaction is expected to close by March 1, 2014.

Manchester markets two drugs that have been approved by the U.S. Food and Drug Administration. Chenodal® (chenodeoxycholic acid -- a synthetic bile acid also known as chenodiol) is indicated for patients suffering from gallstones in whom surgery poses an unacceptable health risk due to disease or advanced age. Vecamyl® (mecamylamine HCI tablets) is indicated for the management of moderately severe to severe essential hypertension and uncomplicated cases of malignant hypertension.

Chenodeoxycholic acid is also the standard of care for cerebrotendinous xanthomatosis (CTX), a rare inborn error of cholesterol metabolism that often causes chronic diarrhea in infants and cataracts in childhood or adolescence and ultimately neurodegeneration caused by formation of fatty yellow nodules (xanthomas) in the brain. If untreated, the disease can cause severe intellectual disability and death. The FDA granted chenodiol orphan designation for CTX in March 2010. Chenodal is the only FDA-approved chenodeoxycholic acid and is only used for CTX.

“We are delighted to have the opportunity to help patients with CTX, an underdiagnosed and deadly disease,” said Martin Shkreli, Founder and Chief Executive Officer of Retrophin. “Almost all patients have avoidable permanent neurological damage, underscoring the need for earlier diagnosis. We also intend to move quickly to pursue FDA approval of Chenodal for CTX.”

Providing revenue guidance for the first time, Retrophin expects 2014 revenues to be in the range of $10 million to $12 million, and 2015 revenues in the range of $19 million to $21 million.

Conference Call Information

Retrophin will host a conference call and webcast (with slides) tomorrow morning, Thursday, February 13, at 8:30 a.m. ET, to discuss the acquisition of Manchester Pharmaceuticals. To participate in the conference call, dial 1-855-219-9219 (U.S.) or 1-315-625-6891 (International), confirmation code 25838792, shortly before 8:30 a.m. The audio webcast and slides can be accessed at www.retrophin.com, in the Events and Presentations section. A replay of the call will be available February 13, 2014 11:30 a.m. ET to February 27, 2014 11:59 p.m. ET. The replay number is 1-855-859-2056 (U.S.) or 1-404-537-3406 (International), confirmation code 25838792.

About Manchester Pharmaceuticals

Manchester Pharmaceuticals, a privately-held specialty pharmaceutical company, is focused on the identification, development, and commercialization of therapeutic modalities to address the special needs of patients with ultra-rare diseases. Manchester markets Chenodal® (chenodiol tablets) and Vecamyl® (mecamylamine tablets) in the U.S. Manchester’s founders and management have extensive combined experience in the rare disease market. For additional information, please visit www.manchesterpharma.com.

About Retrophin

Retrophin is a pharmaceutical company focused on the development, acquisition and commercialization of drugs for the treatment of serious, catastrophic or rare diseases for which there are currently no viable options for patients. The Company's pipeline includes compounds for several catastrophic diseases, including focal segmental glomerulosclerosis (FSGS), pantothenate kinase-associated neurodegeneration (PKAN), schizophrenia, autism, infantile spasms, nephrotic syndrome and others. Retrophin intends to reintroduce Syntocinon Nasal Spray in the U.S. to assist initial postpartum milk ejection. For additional information, please visit www.retrophin.com.

icon url

iwfal

02/12/14 7:14 PM

#174134 RE: biomaven0 #174129

RTRX -

Either it is a deliberate pump or someone got very confused indeed about the right disease or the right drug. No way seven patients could already be dosed - as far as I know there has been no announcement that the drug is in the clinic at all.



I strongly suspect that this report is largely correct. It is right in line with what Shkrelli said they would be doing and on schedule for the timeline he gave in December. (kudos that he is moving smartly into execution!)

1) Shkrelli said they would dose some patients via "Compassionate Use" (i.e. outside a trial) prior to the first trial. Honestly I had reservations that this would be allowed by the FDA - but even in December he continued to assert that it was imminent (in line with previous commits).

2) Since it isn't a trial it doesn't surprise me that it isn't on Clinical Trials.

3) Shkrelli does seem to release information in non-standard ways (e.g. important lawsuit only shows up in 8K - which does happen, but not very common in biotech). And honestly, the impression I get from the conference calls is that his ex-peers are getting more 'context' information than typical. (That always happens to some degree - e.g. calls to IR - but questioners just seem to know a lot more context than I am used to.)
icon url

BTH

02/13/14 10:56 AM

#174162 RE: biomaven0 #174129

The article was sourced by a moron who was watching Facebook forum posts of patients in another PKAN trial and didn't bother to inquire as to what drug it actually is. There is another drug in PKAN patients right now being trialed.

RE-024 has not dosed yet (this week).