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Pacira BioSciences Inc (PCRX)

  • Event
  • May 12, 2022, 12:09 UTC

(10% Negative) PACIRA BIOSCIENCES, INC. (PCRX) Announces Delay in million Trials for managing osteoarthritis Due to Pandemic-Related Challenges, Manufacturing Considerations, Safety Review, Efficacy Assessment

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  • News bot Oct. 1, 2025, 3 p.m.

    📋 PACIRA BIOSCIENCES, INC. (PCRX) - Clinical Trial Update

    Filing Date: 2022-05-12

    Accepted: 2022-05-12 08:09:25

    Event Type: Clinical Trial Update

    Event Details:

    Pacira BioSciences Inc (PCRX) Announces Clinical Trial Update Pacira BioSciences Inc (PCRX) provided an update on its clinical development programs. Clinical Development Highlights:
    • Drug Program: million, differences
    • Diseases/Conditions: managing osteoarthritis
    • Update Type: Trial Timeline Adjustment
    • Primary Factors: Pandemic-Related Challenges
    • Collaboration: EXPAREL®
      • anticipated by financial analysts or investors, the market price of our shares could decline; the impact of the COVID-19 pandemic on elective surgeries, our manufacturing and supply chain, global and United States economic conditions, and our business, including our revenues, financial condition and results of operations; the success of our sales and manufacturing efforts in support of the commercialization of EXPAREL, ZILRETTA and iovera° and the rate and degree of market acceptance of EXPAREL, ZILRETTA and iovera°; the size and growth of the potential markets for EXPAREL, ZILRETTA and iovera° and our ability to serve those markets; our plans to expand the use of EXPAREL, ZILRETTA and iovera° to additional indications and opportunities, and the timing and success of any related clinical trials for EXPAREL, ZILRETTA and iovera°; the commercial success of EXPAREL, ZILRETTA and iovera°; the related timing and success of United States Food and Drug Administration supplemental New Drug Applications, and premarket notification 510(k)s; the related timing and success of European Medicines Agency Marketing Authorization Applications; our plans to evaluate, develop and pursue additional product candidates utilizing our proprietary multivesicular liposome (pMVL) drug delivery technology; the approval of the commercialization of our products in other jurisdictions; clinical trials in support of an existing or potential pMVL-based product; our commercialization and marketing capabilities, our ability to successfully construct an additional EXPAREL manufacturing suite in San Diego, California; our ability to successfully complete a ZILRETTA capacity expansion project in Swindon, England; the outcome of any litigation; the ability to successfully integrate Flexion or any future acquisitions into our existing business; the recoverability of our deferred tax assets; and assumptions associated with contingent consideration payments; and factors discussed in the “Risk Factors” of our most recent Annual Report on Form 10-K and in other filings that we periodically make with the Securities and Exchange Commission. In addition, the forward-looking statements included in this press release represent our views as of the date of this press release. Important factors could cause actual results to differ materially from those indicated or implied by forward-looking statements, and as such we anticipate that subsequent events and developments will cause our views to change. However, while we may elect to update these forward-looking statements at some point in the future, we specifically disclaim any obligation to do so, except as required by law. These forward-looking statements should not be relied upon as representing our views as of any date subsequent to the date of this press release.###Investor Contact:Susan Mesco, (973) 451-4030

    💼 Business Developments:

    • Partnership: Not available
    • Acquisition
    • Licensing: Not available
    • Regulatory Approval
    • Executive Changes: Not available

    Structured Data:

    • Company Name: Pacira BioSciences Inc
    • CIK: 0001396814
    • Ticker Symbol: PCRX
    • Period End Date: 2022-05-12
    • Document Type: 8-K

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