Data from Uncontrolled Gout Case Series Supports Immunomodulation with KRYSTEXXA® (pegloticase injection) Strategy to Optimize Treatment Outcomes
DUBLIN--(BUSINESS WIRE)--Nov 11, 2019--
Horizon Therapeutics plc (Nasdaq: HZNP) today announced the presentation of a patient case series at the American College of Rheumatology (ACR) Annual Meeting illustrating that the addition of methotrexate to a course of therapy with KRYSTEXXA® (pegloticase injection) may help more people with chronic gout refractory to conventional therapies – also known as uncontrolled gout – achieve response to treatment. In addition, Horizon will present data describing the inflammatory impact of uric acid on other organs, including the liver and kidney.
KRYSTEXXA has demonstrated rapid reduction in the serum uric acid level for people with uncontrolled gout; however, as with any biologic, the immune system can sometimes react to the therapeutic proteins, hindering a complete response. Immunomodulators, such as methotrexate, are often co-prescribed with biologics to help reduce this reaction.
The case series presented by John A. Albert, M.D. details his in-practice experience for 10 adult patients with uncontrolled gout who received KRYSTEXXA during or after treatment with methotrexate (either oral or subcutaneous). Methotrexate exposure varied (most received 25 mg of methotrexate subcutaneously every week and nine of the 10 patients started methotrexate prior to receiving KRYSTEXXA). Eight of the 10 patients were complete responders at 24 weeks of therapy. Two patients ceased therapy, one due to loss of response and a mild infusion reaction, and the other due to methotrexate injection-related issues. Treatment was well tolerated for the duration of therapy. Given the importance of this clinical concept, Horizon assisted with the analysis and compilation of the case series. The co-prescription of KRYSTEXXA and methotrexate is investigational and its safety and efficacy have not been established. (Subcutaneous or oral methotrexate exposure and response to pegloticase in uncontrolled gout patients in a community rheumatology practice, Abstract 1236 )
“Despite gout being the most common form of inflammatory arthritis, it is often not treated with urgency that reflects the impact on patients and its serious, chronic and systemic nature,” said John A. Albert, M.D., Rheumatic Disease Center, Glendale, WI. “In order to address the impact of gout for patients like mine, it is important we quickly and effectively decrease the uric acid burden. Adding methotrexate to KRYSTEXXA treatment for patients with uncontrolled gout employs a commonly used immunomodulation strategy by rheumatologists to minimize the immune response and strives to help more patients benefit from a full course of therapy. This case series demonstrates the significant improvement in response rate which can be achieved through this treatment strategy.”
These in-practice insights expand upon earlier clinical evidence of the immunomodulation strategy from independent investigators, presented during the ACR Annual Meeting in 2018 1 as well as the Annual European Congress of Rheumatology (EULAR) earlier in 2019. 2 Horizon is also evaluating the use of methotrexate to increase the response rate with KRYSTEXXA in its immunomodulation trials, the small MIRROR open-label pivotal study initiated in 2018, and the larger MIRROR registrational clinical trial, which was initiated earlier this year.
Additional presentations deliver new insights on the systemic, inflammatory aspects of uric acid and its effects on multiple organ systems.
“Our research efforts are illustrating important indicators of the multi-organ impact of gout, particularly in the liver and kidneys, where uncontrolled gout can contribute to long-term health consequences,” said Jeffrey D. Kent, M.D., FACG, FACP, executive vice president, medical affairs and outcomes research, Horizon. “Combined with other insights at the ACR meeting, this research highlights the need for clinicians to look holistically at their care strategy for people with gout to ensure the disease is well controlled through appropriate treatment regimens.”
About Uncontrolled Gout
Gout is a chronic, progressive inflammatory form of arthritis that is caused by excess uric acid in the body and needs to be managed aggressively. 3 Over time uric acid can build up and form deposits, called tophi, inside the body and joints, which can have harmful effects including causing damage to the underlying bone. Patients with uncontrolled gout continue to have abnormally high levels of uric acid and continued symptoms of gout despite the use of conventional therapies.4 KRYSTEXXA is the only biologic approved by the U.S. Food and Drug Administration (FDA) for the treatment of uncontrolled gout in adult patients.
INDICATIONS AND USAGE
KRYSTEXXA® (pegloticase injection) is a PEGylated uric acid specific enzyme indicated for the treatment of chronic gout in adult patients refractory to conventional therapy.
Gout refractory to conventional therapy occurs in patients who have failed to normalize serum uric acid and whose signs and symptoms are inadequately controlled with xanthine oxidase inhibitors at the maximum medically appropriate dose or for whom these drugs are contraindicated.
Important Limitations of Use: KRYSTEXXA is not recommended for the treatment of asymptomatic hyperuricemia.
IMPORTANT SAFETY INFORMATION
WARNING: ANAPHYLAXIS AND INFUSION REACTIONS
Anaphylaxis and infusion reactions have been reported to occur during and after administration of KRYSTEXXA. Anaphylaxis may occur with any infusion, including a first infusion, and generally manifests within 2 hours of the infusion. However, delayed-type hypersensitivity reactions have also been reported. KRYSTEXXA should be administered in healthcare settings and by healthcare providers prepared to manage anaphylaxis and infusion reactions. Patients should be premedicated with antihistamines and corticosteroids. Patients should be closely monitored for an appropriate period of time for anaphylaxis after administration of KRYSTEXXA. Serum uric acid levels should be monitored prior to infusions, and healthcare providers should consider discontinuing treatment if levels increase to above 6 mg/dL, particularly when 2 consecutive levels above 6 mg/dL are observed.
The risk of anaphylaxis and infusion reactions is higher in patients who have lost therapeutic response.
Concomitant use of KRYSTEXXA and oral urate-lowering agents may blunt the rise of sUA levels. Patients should discontinue oral urate-lowering agents and not institute therapy with oral urate-lowering agents while taking KRYSTEXXA.
In the event of anaphylaxis or infusion reaction, the infusion should be slowed, or stopped and restarted at a slower rate.
Patients should be informed of the symptoms and signs of anaphylaxis and instructed to seek immediate medical care should anaphylaxis occur after discharge from the healthcare setting.
CONTRAINDICATIONS: G6PD DEFICIENCY ASSOCIATED HEMOLYSIS AND METHEMOGLOBINEMIA
Patients should be screened patients for G6PD deficiency prior to starting KRYSTEXXA. Hemolysis and methemoglobinemia have been reported with KRYSTEXXA in patients with G6PD deficiency. KRYSTEXXA should not be administered to these patients.
An increase in gout flares is frequently observed upon initiation of anti-hyperuricemic therapy, including treatment with KRYSTEXXA. If a gout flare occurs during treatment, KRYSTEXXA need not be discontinued. Gout flare prophylaxis with a non-steroidal anti-inflammatory drug (NSAID) or colchicine is recommended starting at least 1 week before initiation of KRYSTEXXA therapy and lasting at least 6 months, unless medically contraindicated or not tolerated.
CONGESTIVE HEART FAILURE
KRYSTEXXA has not been studied in patients with congestive heart failure, but some patients in the clinical trials experienced exacerbation. Caution should be exercised when using KRYSTEXXA in patients who have congestive heart failure, and patients should be monitored closely following infusion.
The most commonly reported adverse reactions in clinical trials with KRYSTEXXA were gout flares, infusion reactions, nausea, contusion or ecchymosis, nasopharyngitis, constipation, chest pain, anaphylaxis and vomiting.
Horizon is focused on researching, developing and commercializing medicines that address critical needs for people impacted by rare and rheumatic diseases. Our pipeline is purposeful: we apply scientific expertise and courage to bring clinically meaningful therapies to patients. We believe science and compassion must work together to transform lives. For more information on how we go to incredible lengths to impact lives, please visit www.horizontherapeutics.com, follow us @HorizonNews on Twitter, like us on Facebook or explore career opportunities on LinkedIn.
This press release contains forward-looking statements, including statements regarding the potential benefits of KRYSTEXXA, including in combination with methotrexate and expectations regarding the MIRROR clinical trial. These forward-looking statements are based on management’s expectations and assumptions as of the date of this press release and actual results may differ materially from those in these forward-looking statements as a result of various factors. These factors include, but are not limited to, risks regarding whether results of the MIRROR trial will be consistent with results of prior trials or Horizon’s expectations, and the risks associated with clinical development of drug candidates. For a further description of these and other risks facing Horizon, please see the risk factors described in Horizon’s filings with the United States Securities and Exchange Commission, including those factors discussed under the caption “Risk Factors” in those filings. Forward-looking statements speak only as of the date of this press release and Horizon undertakes no obligation to update or revise these statements, except as may be required by law.
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PUB: 11/11/2019 08:00 AM/DISC: 11/11/2019 08:01 AM