BRIDGEWATER, N.J., Oct. 29, 2020 /PRNewswire/ — Insmed Incorporated (Nasdaq: INSM), a all-around biopharmaceutical aggregation on a mission to transform the lives of patients with austere and attenuate diseases, today appear banking after-effects for the third division concluded September 30, 2020, and provided a business update.
“I am admiring to address on a absolute advantageous third division for Insmed as we fabricated cogent beforehand beyond our programs while beforehand ARIKAYCE achievement in the U.S. amidst the advancing pandemic,” commented Will Lewis, Chair and Chief Executive Officer of Insmed. “Driven by the efforts of a world-class team, we accomplished several analytical milestones for ARIKAYCE, including business allotment in the European Union, approval of an sNDA that adds allusive adeptness abstracts to our U.S. label, and connected beforehand of our frontline analytic program. Importantly, we additionally avant-garde affairs to admit a global, registrational Phase 3 abstraction of brensocatib in NCFBE and accomplished a Phase 1 abstraction of TPIP. As we attending advanced to 2021, we accept we are well-positioned to backpack this drive advanced and assassinate on our goals.”
Third Division 2020 Banking Results
Recent Corporate Developments & Affairs Highlights
ARIKAYCE All-around Advancement
On October 28, 2020, Insmed appear that the European Commission (EC) had accustomed business allotment for ARIKAYCE Liposomal 590 mg Nebuliser Dispersion for the analysis of nontuberculous mycobacterial (NTM) lung infections acquired by Mycobacterium avium circuitous (MAC) in adults with bound analysis options who do not accept cystic fibrosis (CF). Consideration should be accustomed to official advice on the adapted use of antibacterial agents. The Aggregation affairs to barrage ARIKAYCE aboriginal in Germany, with the United Kingdom and added European markets to follow, accountable to bounded agreement processes.
In Japan, Insmed continues to ahead ablution ARIKAYCE in the boilerplate of 2021, awaiting approval of its new biologic appliance for the analysis of patients with NTM lung ache acquired by MAC who did not abundantly acknowledge to above-mentioned treatment.
ARIKAYCE Characterization Expansion
On October 19, 2020, the U.S. Food and Biologic Administration (FDA) accustomed an sNDA for ARIKAYCE, abacus important adeptness abstracts apropos the backbone and sustainability of adeptness about-face to the ARIKAYCE label. The data, which are from the Phase 3 CONVERT abstraction of ARIKAYCE, authenticate that the accession of ARIKAYCE to guideline-based analysis (GBT) was associated with abiding adeptness about-face through the end of analysis as able-bodied as abiding adeptness about-face three months post-treatment compared with GBT alone.
Insmed additionally continues to beforehand affairs to accompany authoritative approval of ARIKAYCE as a front-line analysis for patients with MAC lung disease. The Aggregation affairs to admit two analytic trials in the fourth division of 2020 that will be conducted in parallel: ENCORE, a cardinal abstraction advised to accomplish the post-marketing claim to acquiesce abounding approval of ARIKAYCE in the U.S., and ARISE, an interventional abstraction advised to validate the patient-reported aftereffect (PRO) apparatus that will be acclimated to admeasurement adeptness in ENCORE.
In September 2020, abstracts from the Phase 2 WILLOW abstraction of brensocatib in patients with NCFBE were appear online in the New England Journal of Medicine and presented during a late-breaking affair at the European Respiratory Society All-embracing Congress 2020.
Insmed charcoal on clue to admit its planned registrational Phase 3 ASPEN balloon of brensocatib in patients with NCFBE by the end of 2020. The Aggregation has additionally appear affairs to beforehand a analytic development affairs for brensocatib in patients with CF.
In September 2020, Insmed appear that it had accomplished a Phase 1 advantageous advance balloon of TPIP in the United States. The cold of this first-in-human distinct ascendance dosage and assorted ascendance dosage abstraction is to appraise the pharmacokinetics and tolerability contour of TPIP. Four dosing strengths accept now been completed. Top-line abstracts from the abounding Phase 1 abstraction are accustomed in the aboriginal division of 2021 and the Aggregation has appear affairs to admit a Phase 2a abstraction in patients with pulmonary arterial hypertension (PAH) in aboriginal 2021.
As of September 30, 2020, Insmed had banknote and banknote equivalents of $588.8 million. The Company’s absolute operating costs for the third division of 2020 were $89.2 million. Adapted operating expenses, a non-GAAP admeasurement authentic below, for the third division of 2020 were $76.8 million.
The Aggregation affairs to abide advance in the afterward key activities in 2020:
U.S. commercialization of ARIKAYCE;
clinical balloon activities, including (a) admission of ENCORE, the cardinal abstraction advised to acquiesce abounding approval of ARIKAYCE in the U.S. and, in parallel, ARISE, the interventional abstraction to validate the PRO apparatus that will be acclimated in ENCORE, (b) admission of the Phase 3 ASPEN abstraction of brensocatib in patients with NCFBE, and (c) the beforehand of TPIP; and
expansion in Japan and Europe to abutment pre-commercial activities for ARIKAYCE in Japan and barrage activities for ARIKAYCE in antecedent European countries.
Insmed will host a appointment alarm alpha today at 8:30 AM Eastern Time. Shareholders and added absorbed parties may participate in the appointment alarm by dialing (833) 340-0284 (domestic) or (236) 712-2425 (international) and referencing appointment ID cardinal 8292364. The alarm will additionally be webcast alive on the Company’s website at www.insmed.com.
A epitomize of the appointment alarm will be attainable about two hours afterwards its achievement through November 12, 2020 by dialing (800) 585-8367 (domestic) or (416) 621-4642 (international) and referencing appointment ID cardinal 8292364. A webcast of the alarm will additionally be archived for 90 canicule beneath the Investor Relations area of the Company’s website at www.insmed.com.
Non-GAAP Banking Measures
In accession to the U.S. generally accustomed accounting attempt (GAAP) results, this antithesis absolution includes adapted operating expenses, a non-GAAP banking measure, which Insmed defines as absolute operating costs beneath stock-based advantage expense, depreciation, acquittal of intangibles and assertive milestones accompanying to ARIKAYCE, which are payable beneath our adapted agreements with Cystic Fibrosis Foundation Therapeutics, Inc. (CFFT). A adaptation of this non-GAAP banking admeasurement to its best anon commensurable GAAP banking admeasurement is presented in the table absorbed to this columnist release.
Management believes that this non-GAAP banking admeasurement is advantageous to both administration and investors in allegory our advancing business and operating performance. Administration believes that accouterment this non-GAAP advice to investors, in accession to the GAAP results, allows investors to appearance our banking after-effects in the way that administration angle banking results. Management does not intend the presentation of this non-GAAP banking admeasurement to be advised in abreast or as a acting for after-effects able in accordance with GAAP. In addition, this non-GAAP banking admeasurement may alter from analogously called measures acclimated by added companies.
ARIKAYCE is accustomed in the United States as ARIKAYCE® (amikacin liposome assimilation suspension) and in the EU as ARIKAYCE® Liposomal 590 mg Nebuliser Dispersion. Accepted all-embracing analysis guidelines acclaim the use of ARIKAYCE for adapted patients. ARIKAYCE is a novel, inhaled, once-daily conception of amikacin, an accustomed antibacterial that was historically administered intravenously and associated with astringent toxicity to hearing, balance, and branch function. Insmed’s proprietary PULMOVANCE™ liposomal technology enables the commitment of amikacin anon to the lungs, area liposomal amikacin is taken up by lung macrophages area the infection resides, while attached systemic exposure. ARIKAYCE is administered already circadian application the Lamira® Nebulizer System bogus by PARI Pharma GmbH (PARI).
About PARI Pharma and the Lamira® Nebulizer System
ARIKAYCE is delivered by a atypical assimilation device, the Lamira® Nebulizer System, developed by PARI. Lamira® is a quiet, carriageable nebulizer that enables able aerosolization of ARIKAYCE via a vibrating, perforated membrane. Based on PARI’s 100-year history alive with aerosols, PARI is committed to advancing assimilation therapies by developing avant-garde commitment platforms and new biologic formulations that assignment calm to advance accommodating care.
Brensocatib is a baby molecule, oral, capricious inhibitor of dipeptidyl peptidase 1 (DPP1) actuality developed by Insmed for the analysis of patients with non-cystic fibrosis bronchiectasis (NCFBE) and added neutrophil-mediated diseases. DPP1 is an agitator amenable for activating neutrophil serine proteases (NSPs), such as neutrophil elastase, in neutrophils back they are formed in the cartilage marrow. Neutrophils are the best accepted blazon of white claret corpuscle and comedy an capital role in antibody abolition and anarchic mediation. In abiding anarchic lung diseases, neutrophils accrue in the airways and aftereffect in boundless alive NSPs that account lung abolition and inflammation. Brensocatib may abatement the damaging furnishings of anarchic diseases such as bronchiectasis by inhibiting DPP1 and its activation of NSPs.
IMPORTANT SAFETY INFORMATION FOR ARIKAYCE IN THE U.S.
WARNING: RISK OF INCREASED RESPIRATORY ADVERSE REACTIONS
ARIKAYCE has been associated with an added accident of respiratory adverse reactions, including hypersensitivity pneumonitis, hemoptysis, bronchospasm, and deepening of basal pulmonary ache that accept led to hospitalizations in some cases.
Hypersensitivity Pneumonitis has been appear with the use of ARIKAYCE in the analytic trials. Hypersensitivity pneumonitis (reported as allergic alveolitis, pneumonitis, interstitial lung disease, allergic acknowledgment to ARIKAYCE) was appear at a college abundance in patients advised with ARIKAYCE added accomplishments dieting (3.1%) compared to patients advised with a accomplishments dieting abandoned (0%). Best patients with hypersensitivity pneumonitis discontinued analysis with ARIKAYCE and accustomed analysis with corticosteroids. If hypersensitivity pneumonitis occurs, abandon ARIKAYCE and administer patients as medically appropriate.
Hemoptysis has been appear with the use of ARIKAYCE in the analytic trials. Hemoptysis was appear at a college abundance in patients advised with ARIKAYCE added accomplishments dieting (17.9%) compared to patients advised with a accomplishments dieting abandoned (12.5%). If hemoptysis occurs, administer patients as medically appropriate.
Bronchospasm has been appear with the use of ARIKAYCE in the analytic trials. Bronchospasm (reported as asthma, bronchial hyperreactivity, bronchospasm, dyspnea, dyspnea exertional, abiding expiration, throat tightness, wheezing) was appear at a college abundance in patients advised with ARIKAYCE added accomplishments dieting (28.7%) compared to patients advised with a accomplishments dieting abandoned (10.7%). If bronchospasm occurs during the use of ARIKAYCE, amusement patients as medically appropriate.
Exacerbations of basal pulmonary disease has been appear with the use of ARIKAYCE in the analytic trials. Exacerbations of basal pulmonary ache (reported as abiding adverse pulmonary ache (COPD), communicable deepening of COPD, communicable deepening of bronchiectasis) accept been appear at a college abundance in patients advised with ARIKAYCE added accomplishments dieting (14.8%) compared to patients advised with accomplishments dieting abandoned (9.8%). If exacerbations of basal pulmonary ache action during the use of ARIKAYCE, amusement patients as medically appropriate.
Anaphylaxis and Hypersensitivity Reactions: Serious and potentially life-threatening hypersensitivity reactions, including anaphylaxis, accept been appear in patients demography ARIKAYCE. Signs and affection accommodate astute admission of bark and mucosal tissue hypersensitivity reactions (hives, itching, flushing, bloated lips/tongue/uvula), respiratory adversity (shortness of breath, wheezing, stridor, cough), gastrointestinal affection (nausea, vomiting, diarrhea, crampy belly pain), and cardiovascular signs and affection of anaphylaxis (tachycardia, low claret pressure, syncope, incontinence, dizziness). Afore analysis with ARIKAYCE is instituted, appraise for antecedent hypersensitivity reactions to aminoglycosides. If anaphylaxis or a hypersensitivity acknowledgment occurs, abandon ARIKAYCE and convention adapted admiring measures.
Ototoxicity has been appear with the use of ARIKAYCE in the analytic trials. Ototoxicity (including deafness, dizziness, presyncope, tinnitus, and vertigo) were appear with a college abundance in patients advised with ARIKAYCE added accomplishments dieting (17%) compared to patients advised with accomplishments regimen alone (9.8%). This was primarily apprenticed by tinnitus (7.6% in ARIKAYCE added accomplishments dieting vs 0.9% in the accomplishments dieting abandoned arm) and blackout (6.3% in ARIKAYCE added accomplishments dieting vs 2.7% in the accomplishments dieting abandoned arm). Closely adviser patients with accepted or doubtable audition or vestibular dysfunction during analysis with ARIKAYCE. If ototoxicity occurs, administer patients as medically appropriate, including potentially alternate ARIKAYCE.
Nephrotoxicity was empiric during the analytic trials of ARIKAYCE in patients with MAC lung ache but not at a college abundance than accomplishments dieting alone. Nephrotoxicity has been associated with the aminoglycosides. Close ecology of patients with accepted or doubtable renal dysfunction may be bare back prescribing ARIKAYCE.
Neuromuscular Blockade: Patients with neuromuscular disorders were not enrolled in ARIKAYCE analytic trials. Patients with accepted or doubtable neuromuscular disorders, such as myasthenia gravis, should be carefully monitored back aminoglycosides may aggravate beef weakness by blocking the absolution of acetylcholine at neuromuscular junctions.
Embryo-Fetal Toxicity: Aminoglycosides can account fetal abuse back administered to a abundant woman. Aminoglycosides, including ARIKAYCE, may be associated with total, irreversible, mutual complete deafness in pediatric patients apparent in utero. Patients who use ARIKAYCE during pregnancy, or become abundant while demography ARIKAYCE should be acquainted of the abeyant hazard to the fetus.
Contraindications: ARIKAYCE is contraindicated in patients with accepted hypersensitivity to any aminoglycoside.
Most Accepted Adverse Reactions: The best accepted adverse reactions in Balloon 1 at an accident ≥5% for patients application ARIKAYCE added accomplishments dieting compared to patients advised with accomplishments dieting abandoned were dysphonia (47% vs 1%), ahem (39% vs 17%), bronchospasm (29% vs 11%), hemoptysis (18% vs 13%), ototoxicity (17% vs 10%), high airway affliction (17% vs 2%), musculoskeletal affliction (17% vs 8%), fatigue and asthenia (16% vs 10%), deepening of basal pulmonary ache (15% vs 10%), diarrhea (13% vs 5%), abhorrence (12% vs 4%), pneumonia (10% vs 8%), cephalalgia (10% vs 5%), agitation (7% vs 5%), airsickness (7% vs 4%), adventurous (6% vs 2%), decreased weight (6% vs 1%), change in sputum (5% vs 1%), and chest ache (5% vs 3%).
Drug Interactions: Avoid accessory use of ARIKAYCE with medications associated with neurotoxicity, nephrotoxicity, and ototoxicity. Some diuretics can enhance aminoglycoside toxicity by altering aminoglycoside concentrations in serum and tissue. Avoid accessory use of ARIKAYCE with ethacrynic acid, furosemide, urea, or intravenous mannitol.
Overdosage: Adverse reactions accurately associated with balance of ARIKAYCE accept not been identified. Astute toxicity should be advised with absolute abandonment of ARIKAYCE, and baseline tests of renal action should be undertaken. Hemodialysis may be accessible in removing amikacin from the body. In all cases of doubtable overdosage, physicians should acquaintance the Regional Poison Control Center for advice about able treatment.
LIMITED POPULATION: ARIKAYCE® is adumbrated in adults, who accept bound or no another analysis options, for the analysis of Mycobacterium avium complex (MAC) lung ache as allotment of a aggregate antibacterial biologic dieting in patients who do not accomplish abrogating sputum cultures afterwards a minimum of 6 afterwards months of a multidrug accomplishments dieting therapy. As alone bound analytic assurance and capability abstracts for ARIKAYCE are currently available, assets ARIKAYCE for use in adults who accept bound or no another analysis options. This biologic is adumbrated for use in a bound and specific citizenry of patients.
This adumbration is accustomed beneath accelerated approval based on accomplishing sputum adeptness about-face (defined as 3 afterwards abrogating account sputum cultures) by Month 6. Analytic account has not yet been established. Connected approval for this adumbration may be accidental aloft analysis and description of analytic account in acknowledging trials.
Limitation of Use: ARIKAYCE has alone been advised in patients with adverse MAC lung ache authentic as patients who did not accomplish abrogating sputum cultures afterwards a minimum of 6 afterwards months of a multidrug accomplishments dieting therapy. The use of ARIKAYCE is not recommended for patients with non-refractory MAC lung disease.
Patients are encouraged to address abrogating ancillary furnishings of decree drugs to the FDA. Visit www.fda.gov/medwatch, or alarm 1–800–FDA–1088. You can additionally alarm the Aggregation at 1-844-4-INSMED.
Please see Full Prescribing Information.
Insmed Incorporated is a all-around biopharmaceutical aggregation on a mission to transform the lives of patients with austere and attenuate diseases. Insmed’s aboriginal bartering artefact is a first-in-disease analysis accustomed in the United States and the European Union to amusement a chronic, debilitating lung disease. The Aggregation is additionally advanced a able-bodied activity of investigational therapies targeting areas of austere unmet need, including neutrophil-mediated anarchic diseases and attenuate pulmonary disorders. Insmed is headquartered in Bridgewater, New Jersey, with a growing brand beyond Europe and in Japan. For added information, appointment www.insmed.com.
This columnist absolution contains advanced statements that absorb abundant risks and uncertainties. “Forward-looking statements,” as that appellation is authentic in the Private Securities Action Ameliorate Act of 1995, are statements that are not absolute facts and absorb a cardinal of risks and uncertainties. Words herein such as “may,” “will,” “should,” “could,” “would,” “expects,” “plans,” “anticipates,” “believes,” “estimates,” “projects,” “predicts,” “intends,” “potential,” “continues,” and agnate expressions (as able-bodied as added words or expressions referencing approaching events, altitude or circumstances) may analyze advanced statements.
The advanced statements in this columnist absolution are based aloft the Company’s accepted expectations and beliefs, and absorb accepted and alien risks, uncertainties and added factors, which may account the Company’s absolute results, achievement and achievements and the timing of assertive contest to alter materially from the results, performance, achievements or timing discussed, projected, advancing or adumbrated in any advanced statements. Such risks, uncertainties and added factors include, amid others, the following: abortion to obtain, or delays in obtaining, authoritative approvals for ARIKAYCE alfresco the U.S. or European Union or for the Company’s artefact candidates in the U.S., Europe, Japan or added markets; abortion to auspiciously commercialize or advance U.S. or EU approval for ARIKAYCE, the Company’s alone accustomed product; business or bread-and-butter disruptions due to catastrophes or added events, including accustomed disasters or accessible bloom crises; appulse of the atypical coronavirus (COVID-19) communicable and efforts to abate its advance on the Company’s business, employees, including key personnel, patients, ally and suppliers; the accident that brensocatib does not prove able or safe for patients in approaching analytic studies, including the ASPEN and STOP-COVID19 studies; uncertainties in the amount of bazaar accepting of ARIKAYCE by physicians, patients, third-party payors and others in the healthcare community; the Company’s disability to admission abounding approval of ARIKAYCE from the FDA, including the accident that the Aggregation will not adapted and auspiciously complete the abstraction to validate a PRO apparatus and complete the acknowledging post-marketing abstraction adapted for abounding approval of ARIKAYCE; disability of the Company, PARI Pharma GmbH (PARI) or the Company’s added third-party manufacturers to accede with authoritative requirements accompanying to ARIKAYCE or the Lamira® Nebulizer System; the Company’s disability to admission able agreement from government or third-party payors for ARIKAYCE or adequate prices for ARIKAYCE; development of abrupt assurance or adeptness apropos accompanying to ARIKAYCE or the Company’s artefact candidates; inaccuracies in the Company’s estimates of the admeasurement of the abeyant markets for ARIKAYCE or its artefact candidates or in abstracts the Aggregation has acclimated to analyze physicians, accustomed ante of accommodating uptake, continuance of accustomed treatment, or accustomed accommodating adherence or cessation rates; the Company’s disability to actualize an able absolute sales and business basement or to accomplice with third parties that action such an basement for administration of ARIKAYCE or any of the Company’s artefact candidates that are accustomed in the future; abortion to admission authoritative approval to aggrandize ARIKAYCE’s adumbration to a broader accommodating population; abortion to auspiciously conduct approaching analytic trials for ARIKAYCE, brensocatib, TPIP and the Company’s added artefact candidates due to the Company’s bound acquaintance in administering preclinical development activities and analytic trials all-important for authoritative approval and its abeyant disability to accept or absorb acceptable patients to conduct and complete the trials or accomplish abstracts all-important for authoritative approval, amid added things; risks that our analytic studies will be delayed or that austere ancillary furnishings will be articular during biologic development; abortion of third parties on which the Aggregation is abased to accomplish acceptable quantities of ARIKAYCE or the Company’s artefact candidates for bartering or analytic needs, to conduct the Company’s analytic trials, or to accede with laws and regulations that appulse the Company’s business or agreements with the Company; the Company’s disability to allure and absorb key cadre or to finer administer the Company’s growth; the Company’s disability to acclimate to its awful aggressive and alteration environment; the Company’s disability to abundantly assure its bookish acreage rights or anticipate acknowledgment of its barter secrets and added proprietary advice and costs associated with action or added affairs accompanying to such matters; restrictions or added obligations imposed on the Aggregation by its agreements accompanying to ARIKAYCE or the Company’s artefact candidates, including its authorization agreements with PARI and AstraZeneca AB, and abortion of the Aggregation to accede with its obligations beneath such agreements; the amount and abeyant reputational accident consistent from action to which the Aggregation is or may become a party, including artefact accountability claims; the Company’s bound acquaintance operating internationally; changes in laws and regulations applicative to the Company’s business, including any appraisement reform, and abortion to accede with such laws and regulations; disability to accord the Company’s absolute acknowledgment and uncertainties with account to the Company’s adeptness to admission approaching capital; and delays in the beheading of affairs to body out an added accomplishment ability accustomed by the adapted authoritative authorities and abrupt costs associated with those plans.
The Aggregation may not absolutely accomplish the results, plans, intentions or expectations adumbrated by the Company’s advanced statements because, by their nature, advanced statements absorb risks and uncertainties because they chronicle to contest and depend on affairs that may or may not action in the future. For added advice about the risks and uncertainties that may affect the Company’s business, amuse see the factors discussed in Item 1A, “Risk Factors,” in the Company’s Annual Address on Form 10-K for the year ended December 31, 2019, the Company’s Quarterly Reports on Form 10-Q for the abode ended March 31, 2020 and June 30, 2020 and any consecutive Aggregation filings with the Securities and Exchange Commission (SEC).
The Aggregation cautions readers not to abode disproportionate assurance on any such advanced statements, which allege alone as of the date of this columnist release. The Aggregation disclaims any obligation, except as accurately adapted by law and the rules of the SEC, to about amend or alter any such statements to reflect any change in expectations or in events, altitude or affairs on which any such statements may be based, or that may affect the likelihood that absolute after-effects will alter from those set alternating in the advanced statements.
Financial Statements and Adaptation Follow
Consolidated Statements of Net Loss
(in thousands, except per allotment data)
Three Months Concluded September 30,
Nine Months Concluded September 30,
Cost of artefact revenues (excluding acquittal of abstract assets)
Research and development
Selling, accustomed and administrative
Amortization of abstract assets
Total operating expenses
Other expense, net
Loss afore assets taxes
Provision for assets taxes
Basic and adulterated net accident per share
Weighted boilerplate basal and adulterated accepted shares outstanding
Consolidated Antithesis Sheets
(in thousands, except par amount and allotment data)
September 30, 2020
December 31, 2019
Cash and banknote equivalents
Prepaid costs and added accepted assets
Total accepted assets
Fixed assets, net
Finance charter right-of-use assets
Operating charter right-of-use assets
Liabilities and shareholders’ equity
Finance charter liabilities
Operating charter liabilities
Other accepted liabilities
Total accepted liabilities
Finance charter liabilities, long-term
Operating charter liabilities, long-term
Other abiding liabilities
Common stock, $0.01 par value; 500,000,000 authorized
shares, 101,803,701 and 89,682,387 issued and outstanding shares at September 30, 2020 and December 31, 2019, respectively
Additional paid-in capital
Accumulated added absolute assets (loss)
Total shareholders’ equity
Total liabilities and shareholders’ equity
Reconciliation of GAAP to Non-GAAP Results
Three Months EndedSeptember 30,
Nine Months EndedSeptember 30,
Total operating costs – GAAP
Stock-based advantage expense
Acquittal of intangibles
CFFT anniversary payments
Adjusted operating costs – Non-GAAP
Argot PartnersLaura Perry or Heather Savelle(212) [email protected]
Mandy FaheySenior Director, Corporate CommunicationsInsmed(732) [email protected]
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SOURCE Insmed Incorporated
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