January 08, 2019
BTG and OMNY Partner to Improve Treatment of Snake Bite Victims

Philadelphia, 08 January 2019

BTG, the global healthcare company, is partnering with OMNY to improve visibility of inventory data for its antivenom product CroFab® using distributed ledger technology. 
 
For the estimated 7,000i individuals bitten by rattlesnakes, copperheads, and cottonmouths in the US each year, “time is tissue” and timely treatment is critical. Patients that are not quickly and appropriately treated are at risk of skin and tissue damage, limb function disability or loss, neurotoxic effects, dangerous internal bleeding, and systemic injury to the heart, stomach, and other organs.  This makes it important to understand and manage antivenom stock levels.
 
CroFab® is the only FDA-approved product to treat all North American pit viper envenomations in adult and pediatric patients.ii,iii It is proven to control local, systemic, and hematologic effects of envenomationii, iv, * and 95% of patients showed a clinical response 1 hour after initial control.v  The product has been used for more than 15 years to treat over 50,000 patients.ii
 
Using the OMNY platform, near real-time data about CroFab® stock levels at participating healthcare institutions will be captured and securely shared with BTG and the Rocky Mountain Poison & Drug Center (RMPDC), and in time will expand to additional healthcare providers and poison control centers. 
 
“OMNY’s technology will help us get patients treated as quickly and safely as possible,” says Amanda Goltz, Vice President of Digital at BTG. “This is a game changing application of new tech with a real, meaningful impact. It’s about getting CroFab® where it needs to go and keeping everyone in the chain informed.”
 
Founded by Dr. Mitesh Rao (CEO), Sean O’Brien (CTO) and Sunny Grewal (COO), OMNY helps drive supply chain efficiencies in healthcare. Their novel distributed ledger technology can help track the lifecycle of a product from receipt to dispensation, and can share that data securely in near real-time among multiple constituents. The OMNY platform has the ability to revolutionize the healthcare supply chain and create unique and powerful partnerships between hospitals and pharmaceutical manufacturers.
 
“As an Emergency Medicine physician, I’ve experienced first-hand how difficult it is to provide patient care without access to the treatment,” says Dr. Rao. “Our platform’s ability to quickly and securely share data and ensure its provenance for all involved, can ensure hospitals are adequately stocked, and poison control centers like RMPDC can help coordinate care for hospitals and first responders.”
 
Goltz said, “Two years ago, we released SnakeBite911, an app for First responders, Emergency clinicians, and bite victims with the goal of getting information where it needed to go. OMNY is helping us get to the next stage in the evolution in making sure our medicines are where it matters for patients.”
 
About OMNY:
OMNY leverages distributed ledger technology to enable near real-time visibility of pharmaceutical inventory and trial data. Data is recorded and stored securely, and can be shared across multiple parties (i.e., trading parties, clinical trial constituents) flexibly and with ease. OMNY has offices in San Francisco and Atlanta, and is backed by leading investors including Social Capital, Kevin Ryan and DNA Capital. To learn more about OMNY, please visit www.omnyhealth.com.
 
About BTG Pharmaceuticals
BTG Pharmaceuticals provides antidotes that counteract the potentially life-threatening effects associated with exposure or overexposure to certain toxins. These acute care products are typically used in emergency rooms and intensive care units to treat patients for whom there are limited or no existing treatment options. We are dedicated to delivering quality medicines that make a real difference to patients through the development, manufacture, and commercialisation of pharmaceutical products. To learn more about BTG Pharmaceuticals, please visit: btgplc.com/pharmaceuticals.
 
For further information contact:
BTG                            
Chris Sampson, Corporate Communications Director
+44 (0)20 7575 1595; Mobile: +44 (0)7773 251 178
 
OMNY
G Sunny Grewal, COO
join@omnyhealth.com
 
IMPORTANT SAFETY INFORMATION:
 
CONTRAINDICATIONS
 
Do not administer CroFab® to patients with a known history of hypersensitivity to any of its components, or to papaya or papain unless the benefits outweigh the risks and appropriate management for anaphylactic reactions is readily available.
 
WARNINGS AND PRECAUTIONS
 
Coagulopathy: In clinical trials, recurrent coagulopathy (the return of a coagulation abnormality after it has been successfully treated with antivenin), characterized by decreased fibrinogen, decreased platelets, and elevated prothrombin time, occurred in approximately half of the patients studied; one patient required re-hospitalization and additional antivenin administration. Recurrent coagulopathy may persist for 1 to 2 weeks or more. Patients who experience coagulopathy due to snakebite should be monitored for recurrent coagulopathy for up to 1 week or longer. During this period, the physician should carefully assess the need for re-treatment with CroFab® and use of any type of anticoagulant or anti-platelet drug.
 
Hypersensitivity Reactions: Severe hypersensitivity reactions may occur with CroFab®. In case of acute hypersensitivity reactions, including anaphylaxis and anaphylactoid reactions, discontinue infusion and institute appropriate emergency treatment. Patients allergic to papain, chymopapain, other papaya extracts, or the pineapple enzyme bromelain may also have an allergic reaction to CroFab®. Follow-up all patients for signs and symptoms of delayed allergic reactions or serum sickness (e.g., rash, fever, myalgia, arthralgia).
 
ADVERSE REACTIONS
 
The most common adverse reactions (incidence ≥ 5% of subjects) reported in the clinical studies were urticaria, rash, nausea, pruritus and back pain. Adverse reactions involving the skin and appendages (primarily rash, urticaria, and pruritus) were reported in 12 of the 42 patients. Two patients had a severe allergic reaction (severe hives and a severe rash and pruritus) following treatment and one patient discontinued CroFab® due to an allergic reaction. Recurrent coagulopathy due to envenomation and requiring additional treatment may occur.
 
To report suspected adverse reactions, contact 1-877-377-3784 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
 
Please see the full Prescribing Information for CroFab®.