The Animal Camp is an ultrarunning club founded by its namesake, Josh “The Animal” Dennis.
If you call your friends to organize a training run when you hear reports of a tropical storm hitting your favorite stretch of singletrack, or equate “flood warnings” with “creek crossings”, this is the club for you.
Our athletes are training to push the limits of ultrarunning. Passion, endurance, and a hunger for adventure are the name of the game. “If it doesn’t hurt, sign us up for something that will”. We are not seeking volume of membership, we are looking to become a meeting place for a Family of ultra runners who share an interest in the camaraderie of trail running and the more hardcore aspects of the sport.
Based in the Mid Atlantic region, our short-term goals are to:
spread interest in ultrarunning;
provide a forum for athletes to share information, plan training programs and organize training runs;
foster the closeknit community that is ultrarunning.
A long-term goal is to organize and host a race or races that capture our unique brand of ultra running – what we call “Animal Camp style”.
Welcome to The Animal Camp – enter at your own risk.
The Animal Camp – RUN LIKE AN ANIMAL!
Want to contact the Camp?
Copyright 2008-2011 theanimalcamp.com All rights reserved.
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Celgene Corporation improvements on Phase II research evaluating apremilast in psoriatic arthritis patients Celgene Company announced that updated outcomes of a phase II, multi-middle, randomized, double-blind, placebo-controlled, three-arm study of apremilast in adult sufferers with psoriatic arthritis were presented today at the American University of Rheumatology 2009 annual meeting in Philadelphia, PA generic tadalafil 20mg . CC-10004-PSA-001 sought to determine the efficacy and protection of apremilast in 204 sufferers at two different dosing regimens – 20mg two times per time or 40mg one time per day compared to placebo after 12 weeks, with 126 patients participating in an extension of the study for an additional 12 weeks . Approximately 60 sufferers did not have the opportunity to take part in the extension due to the timing of its initiation. The extension included 40 individuals that had previously received placebo and had been randomized to receive one of the two dosage regimens of apremilast. For individuals who entered the extension, the ACR20 was 40.0 percent and 39.1 percent for 20mg BID and 40mg QD of apremilast, respectively, at 24 weeks. Additionally, topics that switched from placebo to apremilast in the 12-week expansion achieved an ACR20 of 35.0 percent and 40.0 percent in the 20mg BID and 40mg QD arms, at 24 weeks respectively. Related StoriesAbbVie plans to advance ABT-494 to Phase 3 studies in rheumatoid arthritisYoga improves physical, mental wellbeing of people living with common forms of arthritisImmune system protein has potential to avoid onset of aggressive type of rheumatoid arthritisEarlier in the entire year, the primary phase of PSA-001 demonstrated that 43.5 percent of patients in the 20mg BID and 35.8 percent of individuals in the 40mg QD daily arm> The ACR20 criteria measure a 20 percent improvement in tender and swollen joint counts, and also pain, physical function, an inflammation laboratory marker and overall disease activity. ACR20 is the primary assessment utilized by the U.S. Food and Medication Administration for evaluation of efficacy in psoriatic arthritis, in addition to in rheumatoid arthritis. Based on these total results, we look forward to the larger, pivotal research including higher doses to characterize the efficacy and security of oral apremilast in this crucial inflammatory disease. As announced in February 2008, this dosing schedule can be becoming investigated in a stage IIb research in moderate-to-severe plaque-type psoriasis with results expected in the initial half of 2010. Continue reading
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An interview with Dr Matt SilverCell Therapeutics, Inc. announced today that the U.S. Meals and Drug Administration’s Oncologic Medicines Advisory Committee panel voted unanimously that clinical trial data was not adequate to support approval of pixantrone for individuals with relapsed or refractory intense non-Hodgkin’s lymphoma . Presently, there are no approved drugs for individuals with relapsed or refractory intense NHL that have received two or more prior therapies. Pixantrone will be the first drug accepted by the FDA for this indication. Continue reading
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