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Orphan Druganaut Blog | PROVIDING COMPETITIVE INTELLIGENCE, NEWS, INTERNET BUZZ ON GLOBAL ORPHAN DRUG DEVELOPMENTS & RARE DISEASES

PROVIDING COMPETITIVE INTELLIGENCE, NEWS, INTERNET BUZZ ON GLOBAL ORPHAN DRUG DEVELOPMENTS & RARE DISEASES

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Orphan Druganaut Blog | PROVIDING COMPETITIVE INTELLIGENCE, NEWS, INTERNET BUZZ ON GLOBAL ORPHAN DRUG DEVELOPMENTS & RARE DISEASES | orphandruganaut.wordpress.com Reviews
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Orphan Druganaut Blog | PROVIDING COMPETITIVE INTELLIGENCE, NEWS, INTERNET BUZZ ON GLOBAL ORPHAN DRUG DEVELOPMENTS & RARE DISEASES | orphandruganaut.wordpress.com Reviews

https://orphandruganaut.wordpress.com

PROVIDING COMPETITIVE INTELLIGENCE, NEWS, INTERNET BUZZ ON GLOBAL ORPHAN DRUG DEVELOPMENTS & RARE DISEASES

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orphandruganaut.wordpress.com orphandruganaut.wordpress.com
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FDA Breakthrough Therapy And A Rare Disease: Genzyme’s ERT Olipudase Alfa For Niemann-Pick Disease | Orphan Druganaut Blog

https://orphandruganaut.wordpress.com/2015/06/04/fda-breakthrough-therapy-and-a-rare-disease-genzymes-ert-olipudase-alfa-for-niemann-pick-disease

PROVIDING COMPETITIVE INTELLIGENCE, NEWS, INTERNET BUZZ ON GLOBAL ORPHAN DRUG DEVELOPMENTS and RARE DISEASES. WHAT IS AN ORPHAN PRODUCT? COMMENT/PRIVACY/TERMS and CONDITIONS OF USE POLICIES. FDA Breakthrough Therapy Designation. FDA Breakthrough Therapy And A Rare Disease: Genzyme’s ERT Olipudase Alfa For Niemann-Pick Disease. June 4, 2015. A Sanofi company, announces June 4. NPD Types A and B (ASMD or Acid Sphingomyelinase Deficiency). NPD Type C (NPD Type C). It is approximately 1/150,000 for Type C.

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Orphan Druganaut Blog | PROVIDING COMPETITIVE INTELLIGENCE, NEWS, INTERNET BUZZ ON GLOBAL ORPHAN DRUG DEVELOPMENTS & RARE DISEASES | Page 2

https://orphandruganaut.wordpress.com/page/2

PROVIDING COMPETITIVE INTELLIGENCE, NEWS, INTERNET BUZZ ON GLOBAL ORPHAN DRUG DEVELOPMENTS and RARE DISEASES. WHAT IS AN ORPHAN PRODUCT? COMMENT/PRIVACY/TERMS and CONDITIONS OF USE POLICIES. May 30, 2015. 2 New FDA Orphan Drug Designations: Week of 05/25/15. The chart below identifies 2 new FDA Products Receiving Orphan Designation for the week of 05/25 05/29/15. In ascending Orphan Drug Designation Date order. A Products Receiving Orphan Drug Designation (Week of 05/25 05/29/15). May 29, 2015. The 1st I...

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WHAT IS AN ORPHAN PRODUCT ? | Orphan Druganaut Blog

https://orphandruganaut.wordpress.com/what-is-an-orphan-product

PROVIDING COMPETITIVE INTELLIGENCE, NEWS, INTERNET BUZZ ON GLOBAL ORPHAN DRUG DEVELOPMENTS and RARE DISEASES. WHAT IS AN ORPHAN PRODUCT? COMMENT/PRIVACY/TERMS and CONDITIONS OF USE POLICIES. WHAT IS AN ORPHAN PRODUCT? An orphan product is developed for the treatment of a rare medical condition. Per the European patient advocacy group, EURORDIS. At the Orphanet Portal. Per the FDA Office of Orphan Products Development (OOPD). Orphan products (drugs, biologics, devices, or medical foods) demonstrate promis...

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Patient Advocacy: Top Grant-Giving Disease Foundations | Orphan Druganaut Blog

https://orphandruganaut.wordpress.com/2015/06/05/patient-advocacy-top-grant-giving-disease-foundations-2

PROVIDING COMPETITIVE INTELLIGENCE, NEWS, INTERNET BUZZ ON GLOBAL ORPHAN DRUG DEVELOPMENTS and RARE DISEASES. WHAT IS AN ORPHAN PRODUCT? COMMENT/PRIVACY/TERMS and CONDITIONS OF USE POLICIES. Patient Advocacy: Top Grant-Giving Disease Foundations. June 5, 2015. GEN (Genetic Engineering and Biotechnology News). Publishes an online list of the top 35 Nonprofit Disease Foundations. Top Nonprofit Grant-Giving Disease Foundations. Of Total Expenses Awarded As Grants. Brain And Behavior Research Foundation.

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Friedreich’s Ataxia: Film Premiere | Orphan Druganaut Blog

https://orphandruganaut.wordpress.com/2015/06/01/friedreichs-ataxia-film-premiere

PROVIDING COMPETITIVE INTELLIGENCE, NEWS, INTERNET BUZZ ON GLOBAL ORPHAN DRUG DEVELOPMENTS and RARE DISEASES. WHAT IS AN ORPHAN PRODUCT? COMMENT/PRIVACY/TERMS and CONDITIONS OF USE POLICIES. Friedreich’s Ataxia: Film Premiere. June 1, 2015. Kyle Bryant, a spokesperson for the organization, Friedreich’s Ataxia Research Alliance. FARA), led a team of bicyclists in a race across America. Two Redwood Creek Entertainmen. The World Premiere of the film is scheduled for this Saturday, June 6. Friedreich’s Ataxi...

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nissanbrown.wordpress.com nissanbrown.wordpress.com

Hemophilia Type A | nissanbrown

https://nissanbrown.wordpress.com/2014/07/14/hemophilia-type-a

Just another WordPress.com site. July 14, 2014. Hemophilia at its finest →. Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public). You are commenting using your WordPress.com account. ( Log Out. You are commenting using your Twitter account. ( Log Out. You are commenting using your Facebook account. ( Log Out. You are commenting using your Google account. ( Log Out. Notify me of new comments via email. Back in the hospital.

nissanbrown.wordpress.com nissanbrown.wordpress.com

Hemophilia Daredevil | nissanbrown

https://nissanbrown.wordpress.com/2014/07/18/hemophilia-daredevil

Just another WordPress.com site. July 18, 2014. Walter has severe hemophilia A and continues to do things like this. He’s a daredevil! Hemophilia A: My child is normal. Hemophilia: Giving medicine →. Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public). You are commenting using your WordPress.com account. ( Log Out. You are commenting using your Twitter account. ( Log Out. Notify me of new comments via email. The latest ne...

notsosweets.wordpress.com notsosweets.wordpress.com

“What if Your Healing Comes Through Tears?” | Not So Sweet's

https://notsosweets.wordpress.com/2014/03/04/what-if-trials-of-this-night-are-your-mercies-in-disguise

Not So Sweet's. Neutrophilic Dermatosis, a.k.a. Sweet's Syndrome. What is Sweet’s Syndrome? What is Urticarial Vasculitis? 8220;What if Your Healing Comes Through Tears? This entry was posted on March 4, 2014, in Impact on Life. What’s the point and connection with the post title, video and song? Happened with the really sick. We know that God is faithful to us and doesn’t disappoint, but as humans we place our faith in other things and people besides just God. For example, we place faith and h...My real...

nissanbrown.wordpress.com nissanbrown.wordpress.com

Hemophilia: Giving medicine | nissanbrown

https://nissanbrown.wordpress.com/2014/07/19/hemophilia-giving-medicine

Just another WordPress.com site. July 19, 2014. This is just part one of the steps to giving factor. Back in the hospital →. Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public). You are commenting using your WordPress.com account. ( Log Out. You are commenting using your Twitter account. ( Log Out. You are commenting using your Facebook account. ( Log Out. You are commenting using your Google account. ( Log Out. Economic ...

nissanbrown.wordpress.com nissanbrown.wordpress.com

Walter is tough | nissanbrown

https://nissanbrown.wordpress.com/2013/12/20/walter-is-tough

Just another WordPress.com site. December 20, 2013. We are now approaching Christmas and have been here since before thanksgiving. Walter is a tough guy if I must say so myself. I. Still in the hospital dealing with my childs hemophilia. Hemophilia Type A →. Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public). You are commenting using your WordPress.com account. ( Log Out. Notify me of new comments via email. The latest n...

fibromusculardysplasia.blogspot.com fibromusculardysplasia.blogspot.com

Fibromuscular Dysplasia: February 2014

http://fibromusculardysplasia.blogspot.com/2014_02_01_archive.html

An informal place to help support people afflicted with FMD. Friday, February 28, 2014. Update from Washington DC Rare Disease Day 2014. It is with great joy to announce that today Dr. Collins, NIH Director was presented our petition on behalf of Fibromuscular Dysplasia, Ehlers-Danlos Syndrome, Marfans and Sticklers. The petition was hand delivered in Washington DC by Sarah. Kucharski, Patient and Founder of FMD Chat. And Fran Richmond Saplis. Patient and Advisor to FMDChat. Monday, February 24, 2014.

notsosweets.wordpress.com notsosweets.wordpress.com

Dapsone Risk, Hemolytic Anemia | Not So Sweet's

https://notsosweets.wordpress.com/2013/10/11/dapsone-risk-hemolytic-anemia

Not So Sweet's. Neutrophilic Dermatosis, a.k.a. Sweet's Syndrome. What is Sweet’s Syndrome? What is Urticarial Vasculitis? Dapsone Risk, Hemolytic Anemia. This entry was posted on October 11, 2013, in Autoimmune. Hemolyitic Anemia just one of the risks of taking Dapsone, a commonly used medication treatment for Sweet’s Syndrome, Urticarial Vasculitis, Chronic Urticaria and other skin diseases. 8220;Are the benefits of Dapsone still out-weighing the risks? I could wear my tennis shoes! We had a great time...

notsosweets.wordpress.com notsosweets.wordpress.com

Another New Drug; More Guinea Pigging for Me | Not So Sweet's

https://notsosweets.wordpress.com/2014/04/02/another-new-drug-more-guinea-pigging-for-me

Not So Sweet's. Neutrophilic Dermatosis, a.k.a. Sweet's Syndrome. What is Sweet’s Syndrome? What is Urticarial Vasculitis? Another New Drug; More Guinea Pigging for Me. This entry was posted on April 2, 2014, in Medication. It shouldn’t come as a surprise to me, yet there I sat in shock. “I’ve been doing so well.” Yes, I have these strange new symptoms, but they’re nothing compared to where I was 12 months ago. So, why not keep my magic cocktail longer? It’s not all bad news. Orencia is a shot! A weekly ...

fibromusculardysplasia.blogspot.com fibromusculardysplasia.blogspot.com

Fibromuscular Dysplasia: Patients Advocate for Rare Disease Research in Washington D.C. for Rare Disease Week

http://fibromusculardysplasia.blogspot.com/2014/02/patients-advocate-for-our-rare-disease.html

An informal place to help support people afflicted with FMD. Monday, February 24, 2014. Patients Advocate for Rare Disease Research in Washington D.C. for Rare Disease Week. Dr Francis S. Collins,. With this petition of over 10,000 signatures. Thank you to FMD Chat. For printing and delivering our petition to Washington D.C. Special thank you to Rare Disease Patients: Sarah Kucharski, Fran Saplis RN, and Judy Brown for delivering our petition! Croatian Alliance for Rare Diseases. The Joe Niekro Foundation.

helpforsweetssyndromeuk.wordpress.com helpforsweetssyndromeuk.wordpress.com

Frequently asked questions – Help for Sweet's Syndrome, UK

https://helpforsweetssyndromeuk.wordpress.com/useful-links/faqs

Help for Sweet's Syndrome, UK. Please BEE sweet and buzz for Sweet's. Help us spread the word. Key info: what you need to know. What is Sweet’s syndrome? What kind of condition is Sweet’s syndrome? What causes Sweet’s syndrome? What are the symptoms of Sweet’s syndrome? How is Sweet’s syndrome diagnosed? What is the treatment for Sweet’s syndrome? Medical Articles & Trials. Free Clinical Papers (1). Free Clinical Papers (2). Useful info: contact us & resources. Support Groups & Forum. 7 Can I use essenti...

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Promoting Access to Essential Medicine. Wasienmedizin e.V. - PACEM is a small organization with big ideals! Founded on Mai 19th 2000 the association has brought forward projects all allocated in the health sector in different countries focussing on Afghanistan in the last 10 years. WM eV is belonging to the group of organizations, namely for instance OneWorldHealth. WM eV is organized into two related departments. The non governmental charitable organization depends on donations and volunteer work&#4...

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Orphan Druganaut Blog | PROVIDING COMPETITIVE INTELLIGENCE, NEWS, INTERNET BUZZ ON GLOBAL ORPHAN DRUG DEVELOPMENTS & RARE DISEASES

PROVIDING COMPETITIVE INTELLIGENCE, NEWS, INTERNET BUZZ ON GLOBAL ORPHAN DRUG DEVELOPMENTS and RARE DISEASES. WHAT IS AN ORPHAN PRODUCT? COMMENT/PRIVACY/TERMS and CONDITIONS OF USE POLICIES. June 13, 2015. 10 New FDA Orphan Drug Designations: Week of 06/08/15. The chart below identifies 10 new FDA Products Receiving Orphan Designation for the week of 06/08 06/12/15. In ascending Orphan Drug Designation Date order. A Products Receiving Orphan Drug Designation (Week of 06/08 06/12/15). June 7, 2015. 6 New ...

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Dutch Orphan Drug Network -

Dutch Orphan Drug Network. Voor meer resultaat. LEES VERDER. Wij zijn een onafhankelijk. Netwerk van orphan drug. Specialisten in Nederland. LEES VERDER. Sluit u aan bij ons. Netwerk en deel uw. Kennis over OD in Nederland. LEES VERDER. Tijd om de handen ineen te slaan. Help ons om therapieën voor mensen met een zeldzame ziekte sneller op de markt te brengen. Word nu gratis lid van ons netwerk. Eerste symposium voor jongeren met Von Hippel Lindau. Platencontract voor tiener met botkanker.

orphandrugnetwork.org orphandrugnetwork.org

Dutch Orphan Drug Network -

Dutch Orphan Drug Network. Wij zijn een onafhankelijk. Netwerk van orphan drug. Specialisten in Nederland. LEES VERDER. Voor meer resultaat. LEES VERDER. Sluit u aan bij ons. Netwerk en deel uw. Kennis over OD in Nederland. LEES VERDER. Tijd om de handen ineen te slaan. Help ons om therapieën voor mensen met een zeldzame ziekte sneller op de markt te brengen. Word nu gratis lid van ons netwerk. Eerste symposium voor jongeren met Von Hippel Lindau. Platencontract voor tiener met botkanker.

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Orphan Drugs Homepage

FDA Office of Orphan Products Development. This is spider bait: Ignore it. The various treatments include minoxidil propecia superoxide dismutase and antiandrogens. Signaling redox vascular skin topical vitamin c. Medicines.nu Zyrtec Paxil Rogaine Fosamax Advair Zocor Propecia Accutane Prilosec Effexor. Azmacort Atenolol Baclofen bactrim Benicar Bextra Biaxin Buspar Carisoprodol Celebrex Celexa Cephalexin Cialis Cipro Claritin Clindamycin Clonazepam Clonidine Codeine Concerta Coumadin Crestor hair regrow...

orphandrugs.janiec.info orphandrugs.janiec.info

Orphan DrugsProsperity and Misery by Waldemar Janiec

The discovery of each orphan drug to treat rare diseases led through many paths. Some paths ended with success. others with failure. There were cases that great misfortunes contributed to the discovery of orphan drugs. The showing of the difficulties and ways of searching for orphan drugs will allow for a better understanding of the fate and misery of orphan drugs, which are so very needed by those suffering from rare diseases. On the cover photo: Michał Janiec,. Graphics: Arek Garcia, Cologne 2014.