Item 1.02. | Termination of a Material Definitive Agreement. |
On February 18, 2020, Eagle Holding Company II (“Eagle II”), a Delaware corporation and wholly-owned subsidiary of PPD, Inc. (the “Company”), a Delaware corporation, will redeem all of its outstanding (i) $550 million aggregate principal amount of 7.625%/8.375% Senior PIK Toggle Notes due 2022 (the “Initial Notes”) and (ii) $900 million aggregate principal amount of 7.75%/8.50% Senior PIK Toggle Notes due 2022 (the “Additional Notes” and, together with the Initial Notes, the “Notes”) in accordance with the provisions of the Notes and the indentures governing the Notes. As such, the obligations of Eagle II under the Notes and such indentures will be discharged on that date.
Item 7.01 | RegulationF-D Disclosure |
The Company recently engaged in discussions with certain lenders about the potential of refinancing (i) the existing term loan and revolving credit facilities under its Credit Agreement, dated as of August 18, 2015, among Jaguar Holding Company II, Pharmaceutical Product Development, LLC, Jaguar Holding Company I, LLC, Credit Suisse AG, Cayman Islands Branch, as Administrative Agent, Collateral Agent and L/C Issuer, and each lender from time to time party thereto, as amended, and (ii) the 6.375% Senior Notes due 2023 issued by Jaguar Holding Company II and Pharmaceutical Product Development, LLC with the borrowings under a new term loan and revolving credit facilities.
In connection with such discussions, the Company will be providing certain information to these potential lenders relating to the Company, which was confidential until the date of this filing. Such information is furnished as Exhibit 99.1 to this Current Report onForm 8-K and incorporated herein by reference.
The Company may from time to time engage in further discussions and may refinance, repay, redeem, amend and/or replace, in whole or in part, the Company’s indebtedness. The amount, pricing and other terms of any new credit facilities have not been determined and the Company cannot assure you if, or when, it would enter into such new credit facilities.
The information in this Item 7.01 (including Exhibit 99.1) of this Current Report on Form8-K is being “furnished” and shall not be deemed “filed” for the purposes of Section 18 of the Securities Exchange Act of 1934, as amended, or otherwise subject to the liability of that Section, nor shall it be deemed incorporated by reference in any filing under the Securities Act of 1933, as amended, except as shall be set forth by specific reference in such filing.
Forward Looking Statements
This Current Report on Form8-K contains forward-looking statements. These statements often include words such as “anticipate,” “expect,” “suggest,” “plan,” “believe,” “intend,” “project,” “forecast,” “estimates,” “targets,” “projections,” “should,” “could,” “would,” “may,” “might,” “will,” and other similar expressions. Although the Company believes that these forward-looking statements are based on reasonable assumptions at the time they are made, you should be aware that many factors could affect the Company’s actual financial results, and therefore actual results might differ materially from those expressed in the forward-looking statements. Factors that might materially affect such forward-looking statements include: the fragmented and highly competitive nature of the drug development services industry; changes in trends in the biopharmaceutical industry; the Company’s ability to keep pace with rapid technological changes that could make its services less competitive or obsolete; political, economic and/or regulatory influences and changes; any failure of the Company’s backlog to predict or convert into future revenue; the fact that the Company’s customers can terminate, delay or reduce the scope of their contracts with the Company upon short notice or with no notice; the impact of industry, customer and therapeutic area concentration; the Company’s ability to accurately price the Company’s contracts and manage its costs associated with performance of such contracts; any failures in the Company’s information and communication systems, impacting it or its customers, clinical trial participants or employees; any failure to perform services in accordance with contractual requirements, regulatory standards and ethical standards; the Company’s ability to recruit, retain and motivate key personnel; the Company’s ability to attract suitable investigators or enroll a sufficient number of patients for its customers’ clinical trials; any failure by the Company to comply with numerous privacy laws; the Company’s dependence on third parties for critical goods and support services; the Company’s dependence on its technology network, and the impact from upgrades to the network; any violation of laws, including laws governing