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Fennec Pharmaceuticals Ord Shs T.FRX

Alternate Symbol(s):  FENC

Fennec Pharmaceuticals Inc. is a commercial-stage biopharmaceutical company focused on its product candidate PEDMARK. It sells its product through a field force, including Regional Pediatric Oncology Specialists and medical science liaisons who are helping to educate the medical communities and patients about cisplatin induced ototoxicity and its programs supporting patient access to PEDMARK. PEDMARK is a Food and Drug Administration approved therapy indicated to reduce the risk of ototoxicity associated with cisplatin treatment in pediatric patients with localized, non-metastatic, solid tumors. It is a formulation of sodium thiosulfate in single-dose, ready-to-use vials for intravenous use in pediatric patients. PEDMARK is a therapeutic agent with a dosing paradigm, across two open-label, randomized Phase 3 clinical studies, the Clinical Oncology Group (COG) Protocol ACCL0431 and SIOPEL 6. It has established Fennec HEARS, a single source program designed to connect PEDMARK patients.


TSX:FRX - Post by User

Post by Brinkleyon Aug 19, 2005 8:30am
261 Views
Post# 9432587

Increased Target price $4.60

Increased Target price $4.60 Versant Partners sent out a 12 page report about Adherex and the GSK deal. They beleive that the aquisition of eniluracil has increased the share price substantially. I was interested to see that the analyst used a 50% discount rate when calculating the Present value of cash flows. As we get through the various stages of development this discount rate will drop and the value will rise substantially. Below is part of the report from Versant All values in C$ unless otherwise noted. Symbol: AHX, ADH Exchanges: TSX, AMEX Current Price: $1.80 Previous 1-Year Target (adjusted for share consol): $3.75 New 1-Year Target $4.60 Target Return: 156% SPECULATIVE BUY Industry: Healthcare and Biotechnology Adherex reported fiscal Q2 results, generating a net loss of US$4.6 million in line with our expectations upon considering ongoing Phase Ib/II studies testing its vascular targeting agent Exherin. Sufficient cash to fund Exherin & eniluracil development until Phase II Exherin testing is complete. Quarter-end cash balance was US$12.6 million, and when we add proceeds raised from its recent US$8.5 million equity financing and incorporate our expected Jul/05 burn of about US$1.5 million, we assume the company has about US$20 million to fund Exherin and eniluracil development (see below) until calendar Q3/05, US$3 million of which is expected to provide sufficient capital to conduct all testing required to take eniluracil to Phase III trials, possibly by H1/07. Market responding with indifference to Glaxo deal – so far. Recall that Adherex signed a licensing agreement with GlaxoSmithKline (Glaxo), providing Glaxo an option to develop Exherin (pending positive Phase II data, of course), while Adherex acquired rights to develop 5-ethynyluracil (or eniluracil), an antimetabolite chemotherapy agent shown in multiple preclinical-Phase II studies to improve efficacy of a still-common anticancer drug 5-fluorouracil (5-FU), but unfortunately not in two pivotal Phase IIIs conducted by Glaxo a few years ago. Adherex believes that in partnership with collaborators, its research team identified some key refinements that could improve eniluracil performance in a re-designed Phase III (likely colorectal, breast, or pancreatic cancer) and has a few undisclosed parameters it needs to test before launching into another Phase III trial, probably in H1/07 as stated. Adherex’s Chief Scientific Officer Brian Huber is a Glaxo alumnus, working since 1986 with Wellcome Research Labs (since acquired by Glaxo) who we believe facilitated negotiations. Company Description: Adherex is a biopharmaceutical company focused on the development of cancer therapeutics through its cadherin targeting, vascular targeting technology. Douglas W. Loe, Ph.D, MBA
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