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Viatris Inc (VTRS)

Viatris Inc. operates as a global pharmaceutical and healthcare enterprise. Its business is structured across four primary geographic divisions: Developed Markets, Greater China, JANZ (Japan, Australia, New Zealand), and Emerging Markets. The company offers a comprehensive range of pharmaceutical products, encompassing branded prescription medications, generic and complex generic drugs, biosimilar treatments, and active pharmaceutical ingredients (APIs). These offerings target diverse therapeutic areas, addressing both noncommunicable and infectious diseases. Its biosimilars specifically focus on critical conditions in oncology, immunology, endocrinology, ophthalmology, and dermatology. Furthermore, Viatris's APIs are utilized across numerous drug categories, including antibacterials, central nervous system agents, antihistamines/antiasthmatics, cardiovascular, antivirals, antidiabetics, antifungals, and proton pump inhibitors. Beyond manufacturing medicines, Viatris supports patient well-being through additional services such as diagnostic clinics, educational seminars, and digital tools designed to assist with health management. Products are made available in various forms, including oral solids, injectable solutions, complex dosage formulations, and raw APIs. Viatris distributes these to a broad clientele globally, including retail pharmacies, wholesalers, government bodies, insurance providers, and institutional healthcare facilities. The distribution network involves pharmaceutical wholesalers, retail and institutional pharmacies, mail-order and e-commerce platforms, and specialty pharmacies. The company's extensive portfolio includes prominent brands like Lyrica, Lipitor, Creon, Influvac, Wixela Inhub, EpiPen auto-injector, Fraxiparine, Yupelri, Norvasc, Viagra, AMITIZA, Lipacreon, Effexor, Celebrex, and ARV. Its biosimilar franchises feature products such as Fulphila, Ogivri, Hulio, and SEMGLEE. Viatris Inc. also fosters innovation through strategic collaborations and licensing agreements with partners including Revance Therapeutics, Inc., Momenta Pharmaceuticals, Inc., Theravance Biopharma, Inc., Biocon Ltd., and Fujifilm Kyowa Kirin Biologics Co. Ltd. Founded in 1961, Viatris Inc. maintains its corporate headquarters in Canonsburg, Pennsylvania.

Sector: Pharmaceutical Preparations

Industry: Drug Manufacturers - Specialty & Generic

Viatris Inc. logo

Viatris Inc.

NASDAQ:VTRSHealthcare
-0.86%$19.04
AH$18.91-0.66%vs close
Mkt Cap$21.86B
Float1.15B
O/S1.15B
Vol
$ Vol
RVOL
Inst Own91.5%
SI3.3%
Earnings
Div Yield2.52%
Dilution
Upcoming Catalysts
Phase Distribution
11 lead-sponsored trials·4 active·2 completed
Phase 12
Phase 21
Phase 31
Phase 43
Not applicable4
(21 more as collaborator)

Trials need funding. See this company's dilution risk and cash position.

Clinical Trials
Sponsor role
Status
Phase
  • Phase 4
    Active, not recruiting

    Dymista in Chinese Adolescents

    Treatment with 137 µg azelastine hydrochloride and 50 μg of fluticasone propionate

    Allergic Rhinitis Due to Allergens

    Enrollment
    100
    Start
    May 2026
    Primary Completion
    Oct 2026est.
    Completion
    Oct 2026est.
    NCT07597473
  • Phase 4
    Completed

    Abuse Potential of Oral Gabapentin in Healthy, Non-Drug-Dependent Individuals With Recreational Sedative Drug Use Experience

    Alprazolam (Xanax), Placebo

    Healthy Non-dependent, Recreational Sedative Users

    Enrollment
    44
    Start
    Jun 2026
    Primary Completion
    Aug 2026
    Completion
    Aug 2026
    NCT07777965
  • Phase 4
    Recruiting

    Abuse Potential of Gabapentin Taken Orally Concomitantly With Oxycodone Hydrochloride in Healthy, Non-Drug-Dependent, Recreational Opioid Users

    Placebo, Oxycodone 20mg

    Healthy

    Enrollment
    60
    Start
    Aug 2026
    Primary Completion
    Jan 2027est.
    Completion
    Feb 2027est.
    NCT07813026
  • Phase 3
    Terminated

    A Phase 3 Study to Evaluate the Efficacy and Safety of Pimecrolimus 0.3% Ophthalmic Ointment

    Pimecrolimus 0.3% Ophthalmic Ointment, Placebo Ophthalmic Ointment

    Blepharitis

    Enrollment
    477
    Start
    Apr 2024
    Primary Completion
    Sep 2025
    Completion
    Oct 2025
    NCT06400511
  • Phase 2
    Active, not recruiting

    A Study to Evaluate the Safety,Tolerability,Pharmacokinetics and Pharmacodynamics of Cenerimod in Adult Chinese Participants With Moderate-to-severe Systemic Lupus Erythematosus (SLE)

    cenerimod 4 mg

    SLE - Systemic Lupus Erythematosus

    Enrollment
    15
    Start
    Jan 2026
    Primary Completion
    Oct 2027est.
    Completion
    Oct 2027est.
    NCT07266090
  • Phase 1
    Unknown status

    A Bioequivalence Study of Sacubitril/Valsartan Film-coated Tablets Under Fasting Conditions

    Sacubitril and Valsartan Tablets 97mg/103mg, Entresto (Sacubitril and Valsartan Tablets 97mg/103mg)

    Chronic Heart Failure

    Enrollment
    48
    Start
    Mar 2024est.
    Primary Completion
    Apr 2024est.
    Completion
    Aug 2024est.
    NCT06266988
  • Phase 1
    Unknown status

    A Bioequivalence Study of Sacubitril/Valsartan Film-coated Tablets Under Fasting Conditions

    Sacubitril and Valsartan Tablets 49mg/51mg, Entresto® (Sacubitril and Valsartan Tablets 49mg/51mg)

    Bioequivalence Study

    Enrollment
    48
    Start
    Apr 2024est.
    Primary Completion
    May 2024est.
    Completion
    Sep 2024est.
    NCT06273254
  • Observational
    Completed

    Revatio Special Investigation for Long-term Use in Pediatric Patients

    Sildenafil

    Pulmonary Arterial Hypertension

    Enrollment
    1,023
    Start
    Nov 2017
    Primary Completion
    Aug 2022
    Completion
    Aug 2022
    NCT03364244
  • Observational
    Unknown status

    Post-marketing Surveillance (PMS) to Observe the Safety and Effectiveness of Lyrica CR Extended Release Tablets

    Lyrica CR (Pregabalin)

    Peripheral Neuropathic Pain

    Enrollment
    600
    Start
    Feb 2020
    Primary Completion
    Jul 2022est.
    Completion
    Jul 2022est.
    NCT04171453
  • Observational
    Active, not recruiting

    Observational Study to Evaluate Use of Elidel® in South and East Asian Pediatric Patients With Atopic Dermatitis.

    Elidel 1% Topical Cream

    Mild to Moderate Atopic Dermatitis

    Enrollment
    130
    Start
    Oct 2024
    Primary Completion
    Oct 2026est.
    Completion
    Mar 2027est.
    NCT06052995
  • Observational
    Unknown status

    Safety and Efficacy Evaluation of <Dovprela Tablets 200 mg> by Post-marketing Surveillance

    Dovprela

    Dovprela

    Enrollment
    100
    Start
    Jul 2023
    Primary Completion
    Jun 2026est.
    Completion
    Jun 2026est.
    NCT06471088