Bristol-Myers Squibb To Present New Research Related to the Treatment of Rheumatoid Arthritis Patients With Highly Active, Progressive Disease at the Annual European Congress of Rheumatology (EULAR 2017)

Key analyses focus on treatment outcomes among RA patients with a traditionally poor prognosis

ORENCIA® (abatacept) continuing research underscores Bristol-Myers Squibb’s commitment to advancing the science of modulating the body’s immune response to treat disease

PRINCETON, N.J.--()--Bristol-Myers Squibb Company (NYSE:BMY) today confirmed that 23 abstracts related to ORENCIA® (abatacept), including new data on the role of biomarkers and MRI in RA patient identification and treatment, will be presented at the Annual European Congress of Rheumatology (EULAR 2017), June 14-17 in Madrid, Spain. The Company also will share first-in-human data from BMS-986165, an investigational TYK2 inhibitor.

Bristol-Myers Squibb has played a leading role for more than two decades in discovering and developing medicines designed to help modulate the body’s immune response to treat disease. The abstracts from Bristol-Myers Squibb accepted for EULAR 2017 include three practice-informing analyses pertaining to ORENCIA treatment responses in patients with highly active, progressive rheumatoid arthritis (RA), who traditionally have a poor prognosis. 1-3

  • A post hoc analysis of the phase 3 AGREE* clinical trial showing that among patients with early, erosive RA, treatment with ORENCIA + MTX (vs. MTX alone) resulted in higher seroconversion rates.2 Seroconversion refers to the RA autoantibodies ACPA and RF – anti-citrullinated protein antibodies and rheumatoid factor – falling to undetectable levels among patients who entered the trial with measurable (seropositive) levels.2 ACPA and RF are biomarkers associated with poor prognosis in RA.2 The full data analysis will be featured in a poster tour on Friday, June 16, from 11:45 – 13:30 CET.
  • A post hoc analysis of the phase 3b AVERT** study (MTX versus Orencia+MTX) evaluating the proportion of patients achieving remission at 12 months as measured by baseline MRI-detected inflammation status.3 The analysis explored the response of patients with higher inflammation levels at baseline – as measured by MRI – versus patients with lower baseline levels.3 The full data analysis will be featured in an oral presentation on Friday, June 16, at 10:30 CET.
  • A post hoc analysis of the phase 3b AMPLE*** study that investigated the efficacy of ORENCIA+MTX versus the TNF inhibitor adalimumab+MTX in patients with seropositive, erosive early RA.1 The analysis looked at differences in treatment effect between the two regimens among patients with seropositive, erosive early RA. The full data analysis will be featured in a poster tour on Saturday, June 17, from 10:15 – 12:00 CET.

The research Bristol-Myers Squibb is presenting at EULAR 2017 shows our commitment to advancing scientific understanding of how biomarkers and tools, such as MRI, can be used to guide patient selection and treatment in highly active, progressive rheumatoid arthritis,” said Brian J. Gavin, Vice President, ORENCIA Development Lead at Bristol-Myers Squibb. “Importantly, the research also yields critical insights into the role of modulating the body’s immune system in rheumatoid arthritis and potentially other autoimmune conditions where we are committed to making a meaningful, positive impact on patients’ lives.”

In RA, the body’s immune system mistakenly attacks the joints.4 The costimulation blockade of ORENCIA prevents T-cell activation and the resulting cascade of events that contribute to joint destruction.

The full listing of abstracts Bristol-Myers Squibb will present at EULAR 2017, including data and analyses in rheumatoid arthritis, polyarticular juvenile idiopathic arthritis and psoriatic arthritis, follows. Complete abstracts can be accessed online here.

       
Abstract Title     Presentation Date and Time
Oral Presentations
OP0284: Evaluation of the Impact of Baseline     Friday, June 16
Levels of MRI-Detected Inflammation on Treatment 10:30 CET
Response in Early, Seropositive, MTX-Naïve RA:
Data from the AVERT Trial      
OP0223: Abatacept in the Treatment of Active Friday, June 16
Psoriatic Arthritis: 1-Year Results from a Phase 11:30 CET
III Study      
OP0058: Improvement in Patient-Reported Outcomes Wednesday, June 14
in Patients with Polyarticular-Course Juvenile 17:25 CET
Idiopathic Arthritis and Inadequate Response to
Biologic or Non-Biologic Disease-Modifying
Antirheumatic Drugs Treated with SC Abatacept      
OP0101: Risk of Opportunistic Infections in Thursday, June 15
Patients with Rheumatoid Arthritis Initiating 10:50 CET
Abatacept: Analysis of all Available Clinical
Trial Data      
 
Poster Tours
FRI0219: Association Between Seroconversion Friday, June 16
Status and Clinical Outcomes Following Treatment 11:45 – 13:30 CET
with Abatacept in Combination with Methotrexate
Compared with Methotrexate Alone in Patients
with Early Rheumatoid Arthritis and Poor
Prognostic Indicators      
SAT0041: Efficacy of Abatacept versus Adalimumab Saturday, June 17
in Patients with Seropositive, Erosive Early RA: 10:15 – 12:00 CET
Analysis of a Randomized Controlled Clinical
Trial (AMPLE)      
SAT0177: Safety Events are Similar with Abatacept Saturday, June 17
Versus Placebo Treatment in RA: Results from 10:15 – 12:00 CET
Integrated Data Analysis from Nine Clinical
Trials      
FRI0129: Comparative Safety of Biologic DMARD Friday, June 16
Initiation in RA: A Population-Based 11:45 – 13:30 CET
Observational Study of Malignancy Risk      
SAT0226: A First-in-Human, Study of BMS-986165, a Saturday, June 17
Selective, Potent, Allosteric Small Molecule 10:15 – 12:00 CET
Inhibitor of Tyrosine Kinase 2      
 
Poster Presentations
FRI0245: Abatacept Retention Rates and Prognostic Friday, June 16
Factors of Retention in Patients with Rheumatoid 11:45 – 13:30 CET
Arthritis: 2-Year Results from the Real-world
ACTION Study      
THU0104: Both MRI and HAQ-DI Can Predict Relapses Thursday, June 15
Following all Treatment Withdrawal in MTX-Naïve 11:45 – 13:30 CET
Patients with RA in Remission after 12 Months of
Abatacept Therapy in the AVERT Trial      
THU0725-HPR: Cost Effectiveness Analysis of Thursday, June 15
Abatacept Compared with TNF Inhibitors in 11:45 – 13:30 CET
Patients who are Positive for Anti-Citrullinated
Protein Antibodies Based on Results from an
Observational Trial      
FRI0232: Treatment Effects of Abatacept and Anti- Friday, June 16
TNF in Patients with RA with Poor Prognostic 11:45 – 13:30 CET
Factors: Data from Community Rheumatology
Clinics      
SAT0188: First-Line Treatment Patterns of Saturday, June 17
Patients with Rheumatoid Arthritis who are Anti- 10:15 – 12:00 CET
Cyclic Citrullinated Peptide Antibody Positive
Versus Negative      
FRI0223: Anti-CCP is an Independent Predictor of Friday, June 16
12-Month EULAR Response in Patients with RA 11:45 – 13:30 CET
treated with Abatacept      
THU0626: Cost-Effectiveness of Early Treatment of Thursday, June 15
ACPA Positive Rheumatoid Arthritis Patients with 11:45 – 13:30 CET
Abatacept      
THU0089: M-DAS28, DAS28 (CRP) and RAPID3 Scores Thursday, June 15
at Baseline are Good Predictors of Radiographic 11:45 – 13:30 CET
Disease Progress at 1 and 2 Years: Data from the
AMPLE Trial      
SAT0197: Treatment Outcomes with Anti-TNF and Saturday, June 17
Non-Anti-TNF Disease-Modifying Therapy by 10:15 – 12:00 CET
Baseline Body Mass Index      
FRI0230: Retention Rates of TNF Inhibitors and Friday, June 16
Abatacept Used as a First Biologic DMARD in the 11:45 – 13:30 CET
Treatment of Rheumatoid Arthritis: 8 Years of
Experience from the RHUMADATA® Registry      
SAT0468: Presence of Poor Prognostic Factors May Saturday, June 17
Predict Response to Abatacept in Patients with 10:15 – 12:00 CET
Active Psoriatic Arthritis: Results from a Post
Hoc Analysis from a Phase III Study      
FRI0520: Improved Patient-Reported Outcomes in Friday, June 16
Psoriatic Arthritis Patients Treated with 11:45 – 13:30 CET
Abatacept: Results from a Phase III Trial      
FRI0499: Real-World Study on the Patterns and Friday, June 16
Cost of Treatment Failure in Patients with 11:45 – 13:30 CET
Psoriatic Arthritis Using U.S. Claims Data      
THU0534: Baseline Characteristics and Descriptive Thursday, June 15
Safety Data of Intravenous Abatacept-Treated 11:45 – 13:30 CET
Patients with Juvenile Idiopathic Arthritis in a
U.S. Healthcare Claims Database      
FRI0106: Results of a Systematic Literature Friday, June 16
Review of Prognostic Factors in Rheumatoid 11:45 – 13:30 CET
Arthritis as a Basis for a Prospective
Rheumatologists Survey      
 

About Rheumatoid Arthritis

Rheumatoid arthritis (RA) is a systemic, chronic, autoimmune disease characterized by inflammation in the lining of joints (or synovium), causing joint damage with chronic pain, stiffness, and swelling.4-5 RA causes limited range of motion and decreased joint function.4-5 The condition is more common in women than in men, who account for 75% of patients diagnosed with RA.4-5

About Orencia

Orencia is indicated for reducing signs and symptoms, inducing major clinical response, inhibiting the progression of structural damage, and improving physical function in adult patients with moderately to severely active rheumatoid arthritis. Orencia may be used as monotherapy or concomitantly with disease-modifying antirheumatic drugs (DMARDs) other than tumor necrosis factor (TNF) antagonists.

Orencia is indicated for reducing signs and symptoms in patients 2 years of age and older with moderately to severely active polyarticular juvenile idiopathic arthritis. Orencia may be used as monotherapy or concomitantly with methotrexate (MTX).

Orencia should not be administered concomitantly with TNF antagonists. Orencia is not recommended for use concomitantly with other biologic rheumatoid arthritis (RA) therapy, such as anakinra.

Orencia is intended for use under the guidance of a physician or healthcare practitioner.

Indications/Usage and Important Safety Information for ORENCIA® (abatacept)

Indication and Usage

Adult Rheumatoid Arthritis (RA): ORENCIA® (abatacept) is indicated for reducing signs and symptoms, inducing major clinical response, inhibiting the progression of structural damage, and improving physical function in adult patients with moderately to severely active RA. ORENCIA may be used as monotherapy or concomitantly with disease-modifying, anti-rheumatic drugs (DMARDs) other than tumor necrosis factor (TNF) antagonists.

Juvenile Idiopathic Arthritis (JIA): ORENCIA® (abatacept) is indicated for reducing signs and symptoms in patients aged 2 years of age and older with moderately to severely active polyarticular JIA. ORENCIA may be used as monotherapy or concomitantly with methotrexate (MTX).

Important Limitations of Use: ORENCIA should not be administered concomitantly with TNF antagonists, and is not recommended for use concomitantly with other biologic RA therapy, such as anakinra.

Important Safety Information for ORENCIA® (abatacept)

Concomitant Use with TNF Antagonists: Concurrent therapy with ORENCIA and a TNF antagonist is not recommended. In controlled clinical trials, adult patients receiving concomitant intravenous ORENCIA and TNF antagonist therapy experienced more infections (63%) and serious infections (4.4%) compared to patients treated with only TNF antagonists (43% and 0.8%, respectively), without an important enhancement of efficacy.

Hypersensitivity: Anaphylaxis or anaphylactoid reactions can occur during or after an infusion and can be life-threatening. There were 2 cases (<0.1%; n=2688) of anaphylaxis or anaphylactoid reactions in clinical trials with adult RA patients treated with intravenous ORENCIA. Other reactions potentially associated with drug hypersensitivity, such as hypotension, urticaria, and dyspnea, each occurred in <0.9% of patients. There was one case of a hypersensitivity reaction with ORENCIA in JIA clinical trials (0.5%; n=190). In postmarketing experience, a case of fatal anaphylaxis following the first infusion of ORENCIA was reported. Appropriate medical support measures for treating hypersensitivity reactions should be available for immediate use. If an anaphylactic or other serious allergic reaction occurs, administration of ORENCIA should be stopped immediately and permanently discontinued, with appropriate therapy instituted.

Infections: Serious infections, including sepsis and pneumonia, have been reported in patients receiving ORENCIA. Some of these infections have been fatal. Many of the serious infections have occurred in patients on concomitant immunosuppressive therapy which, in addition to their underlying disease, could further predispose them to infection. Caution should be exercised in patients with a history of infection or underlying conditions which may predispose them to infections. Treatment with ORENCIA should be discontinued if a patient develops a serious infection. Patients should be screened for tuberculosis and viral hepatitis in accordance with published guidelines, and if positive, treated according to standard medical practice prior to therapy with ORENCIA.

Immunizations: Live vaccines should not be given concurrently with ORENCIA or within 3 months of its discontinuation. The efficacy of vaccination in patients receiving ORENCIA is not known. ORENCIA may blunt the effectiveness of some immunizations. It is recommended that JIA patients be brought up to date with all immunizations in agreement with current immunization guidelines prior to initiating therapy with ORENCIA.

Use in Patients with Chronic Obstructive Pulmonary Disease (COPD): Adult COPD patients treated with ORENCIA developed adverse events more frequently than those treated with placebo (97% vs 88%, respectively). Respiratory disorders occurred more frequently in patients treated with ORENCIA compared to those on placebo (43% vs 24%, respectively), including COPD exacerbation, cough, rhonchi, and dyspnea. A greater percentage of patients treated with ORENCIA developed a serious adverse event compared to those on placebo (27% vs 6%), including COPD exacerbation [3 of 37 patients (8%)] and pneumonia [1 of 37 patients (3%)]. Use of ORENCIA in patients with RA and COPD should be undertaken with caution, and such patients monitored for worsening of their respiratory status.

Blood Glucose Testing: ORENCIA for intravenous administration contains maltose, which may result in falsely elevated blood glucose readings on the day of infusion when using blood glucose monitors with test strips utilizing glucose dehydrogenase pyrroloquinoline quinone (GDH-PQQ). Consider using monitors and advising patients to use monitors that do not react with maltose, such as those based on glucose dehydrogenase nicotine adenine dinucleotide (GDH-NAD), glucose oxidase or glucose hexokinase test methods. ORENCIA for subcutaneous (SC) administration does not contain maltose; therefore, patients do not need to alter their glucose monitoring.

Pregnancy: There are no adequate and well-controlled studies of ORENCIA use in pregnant women and the data with ORENCIA use in pregnant women are insufficient to inform on drug-associated risk. A pregnancy registry has been established to monitor pregnancy outcomes in women exposed to ORENCIA during pregnancy. Healthcare professionals are encouraged to register patients by calling 1-877-311-8972.

Lactation: There is no information regarding the presence of abatacept in human milk, the effects on the breastfed infant, or the effects on milk production. However, abatacept was present in the milk of lactating rats dosed with abatacept.

Most Serious Adverse Reactions: Serious infections (3% ORENCIA vs 1.9% placebo) and malignancies (1.3% ORENCIA vs 1.1% placebo).

Malignancies: The overall frequency of malignancies was similar between adult patients treated with ORENCIA or placebo. However, more cases of lung cancer were observed in patients treated with ORENCIA (0.2%) than those on placebo (0%). A higher rate of lymphoma was seen compared to the general population; however, patients with RA, particularly those with highly active disease, are at a higher risk for the development of lymphoma. The potential role of ORENCIA in the development of malignancies in humans is unknown.

Most Frequent Adverse Events (≥10%): Headache, upper respiratory tract infection, nasopharyngitis, and nausea were the most commonly reported adverse events in the adult RA clinical studies. Other events reported in ≥5% of JIA patients were diarrhea, cough, pyrexia, and abdominal pain. In general, the adverse events in pediatric patients were similar in frequency and type to those seen in adult patients.

Note concerning ORENCIA administration options: Intravenous dosing has not been studied in patients younger than 6 years of age. The safety and efficacy of ORENCIA ClickJect Autoinjector for subcutaneous injection has not been studied in patients under 18 years of age.

Please see Full Prescribing Information at http://packageinserts.bms.com/pi/pi_orencia.pdf.

ORENCIA® (abatacept) is a registered trademark of Bristol-Myers Squibb Company.

About Bristol-Myers Squibb Immunoscience

With a robust pipeline of immunomodulatory therapies, Bristol-Myers Squibb is committed to the discovery and development of transformational medicines that could lead to long-term remission in patients with autoimmune diseases. As we discover more about the immune system in such diseases with substantial unmet medical needs, the potential for developing novel therapies that target specific pathways in the immune system continues to drive our research efforts.

About Bristol-Myers Squibb

Bristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. For more information about Bristol-Myers Squibb, visit us at BMS.com or follow us on LinkedIn, Twitter, YouTube and Facebook.

Bristol-Myers Squibb Forward-Looking Statement

This press release contains "forward-looking statements" as that term is defined in the Private Securities Litigation Reform Act of 1995 regarding the research, development and commercialization of pharmaceutical products. Such forward-looking statements are based on current expectations and involve inherent risks and uncertainties, including factors that could delay, divert or change any of them, and could cause actual outcomes and results to differ materially from current expectations. No forward-looking statement can be guaranteed. Forward-looking statements in this press release should be evaluated together with the many uncertainties that affect Bristol-Myers Squibb's business, particularly those identified in the cautionary factors discussion in Bristol-Myers Squibb's Annual Report on Form 10-K for the year ended December 31, 2016 in our Quarterly Reports on Form 10-Q and our Current Reports on Form 8-K. Bristol-Myers Squibb undertakes no obligation to publicly update any forward-looking statement, whether as a result of new information, future events or otherwise.

*Abatacept study to Gauge Remission and joint damage progression in MTX-naive patients with Early Erosive RA

**Assessing Very Early Rheumatoid Arthritis Treatment

***Abatacept versus AdaliMumab ComParison in BioLogic-NaivE RA Subjects with Background Methotrexate

References

1. Fleischmann R., Weinblatt M., Ahmad H., et al. Efficacy of Abatacept Versus Adalimumab in Patients with Serepositive, Erosive Early RA: Analysis of a Randomized Controlled Clinical Trial (AMPLE). EULAR 2017 Abstract.

2. Jansen D., Emery P., Smolen J, et al. Association Between Conversation to ACPA/RD Serenegative Status and Clinical Outcomes Following Treatment with Abatacept in Combination with Methotrexate Compared with Methtrexate Alone in Patients with Early Rheumatoid Arthritis and Poor Prognostic Indicator. EULAR 2017 Abstract.

3. Ahmad H., Baker J., Emery P., et al. Evaluation of the Impact of Baseline Levels of MRI-Detected Inflammation of Treatment Response in Early, Seropositive, MTX-Naïve RA: Data from AVERT Trial. EULAR 2017 Abstract.

4. American College of Rheumatology. Rheumatoid Arthritis. https://www.rheumatology.org/i-am-a/patient-caregiver/diseases-conditions/rheumatoid-arthritis. Accessed May 11, 2017.

5. Centers for Disease Control and Prevention. Rheumatoid Arthritis Fact Sheet. https://www.cdc.gov/arthritis/basics/rheumatoid-arthritis.html. Accessed May 11, 2017

Contacts

Bristol-Myers Squibb Company
Media:
Robert Perry, 407-492-4616
rob.perry@bms.com
or
Investors:
Tim Power, 609-252-7509
timothy.power@bms.com
or
Bill Szablewski, 609-252-5894
william.szablewski@bms.com

Release Summary

Bristol-Myers Squibb To Present New Research Related to the Treatment of Rheumatoid Arthritis Patients With Highly Active, Progressive Disease EULAR

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Contacts

Bristol-Myers Squibb Company
Media:
Robert Perry, 407-492-4616
rob.perry@bms.com
or
Investors:
Tim Power, 609-252-7509
timothy.power@bms.com
or
Bill Szablewski, 609-252-5894
william.szablewski@bms.com