Royalty Pharma Reports Q4 2020 and Full-Year Results
- Double-digit growth in Net cash provided by operating activities (GAAP) and Adjusted Cash Flow(2)
$2.4 billion of acquisitions announced in 2020; maintained leading share of biopharma royalty funding market- Increasing outlook for 2020-2025 Adjusted Cash Receipts(1) CAGR to 7%-10%
“Royalty Pharma achieved a number of major milestones in 2020,” said
GAAP financial results demonstrate continued strong operating cash flow and revenue growth
- Cash from operating activities increased 18% in the fourth quarter; 22% for the full year (on a pro forma basis).
- Cash used in investing activities of $832 million in the fourth quarter;
$2,759 million for the full year. - Cash (used) provided by financing activities of (
$277 million ) in the fourth quarter;$1,487 million for the full year. - Total income and other revenues of $572 million in the fourth quarter;
$2,122 million for the full year.
Non-GAAP financial results (on a pro forma basis) driven by strong, broad-based growth across the portfolio
- Adjusted Cash Receipts(1) grew 9% to
$484 million in the fourth quarter and 1% to$1,800 million in 2020, driven primarily by the cystic fibrosis franchise, Imbruvica and Promacta, despite royalty expirations for mature products. - Adjusted Cash Flow(2) grew 22% to $423 million in the fourth quarter and 15% to
$1,483 million for the full year.
Expanded portfolio with innovative, long duration therapies across diverse therapeutic areas
- Eight transactions announced in 2020 for 12 potentially transformative therapies across five therapeutic areas.
- Recent royalty acquisitions for innovative therapies: Johnson & Johnson’s seltorexant and BioCryst’s Orladeyo.
Financial guidance for 2021 (excludes contributions from new investments)
Royalty Pharma anticipates full-year 2021 Adjusted Cash Receipts(1) to be between$1,910 million and$1,960 million , excluding new transactions announced subsequent to the date of this release.
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(unaudited) | ||||||
($ and shares in millions) | 2020 | 2019 Pro Forma(3) |
Change | 2020 | 2019 Pro Forma(3) |
Change |
Net cash provided by operating activities (GAAP) | 566 | 478 | 18% | 2,035 | 1,673 | 22% |
Net cash used in investing activities (GAAP) | (832) | n/a | n/a | (2,759) | n/a | n/a |
Net cash (used in)/provided by financing activities (GAAP) | (277) | n/a | n/a | 1,487 | n/a | n/a |
Total income and other revenues (GAAP) | 572 | 457 | 25% | 2,122 | 1,814 | 17% |
Adjusted Cash Receipts(1) (non-GAAP) | 484 | 446 | 9% | 1,800 | 1,776 | 1% |
Adjusted Cash Flow(2) (non-GAAP) | 423 | 347 | 22% | 1,483 | 1,290 | 15% |
Fully diluted shares outstanding as of |
607 | n/a | n/a | 607 | n/a | n/a |
Fourth quarter of 2020 financial results
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||||||||
(unaudited) | ||||||||
($ in millions) | 2020 | 2019 Pro forma(3) |
Change | |||||
Net cash provided by operating activities (GAAP) | 566 | 478 | 18% | |||||
Royalty Receipts: | Marketer: | Therapeutic Area: | ||||||
Cystic fibrosis franchise | Vertex | Rare disease | 159 | 116 | 37% | |||
Tysabri | Biogen | Neurology | 93 | 85 | 10% | |||
Imbruvica | AbbVie, J&J | Cancer | 85 | 76 | 12% | |||
HIV franchise | Gilead, others | Infectious disease | 78 | 71 | 10% | |||
Januvia, Janumet, Other DPP-IVs | Merck & Co., others | Diabetes | 40 | 36 | 11% | |||
Xtandi | Pfizer, Astellas | Cancer | 39 | 34 | 16% | |||
Promacta | Novartis | Hematology | 42 | 36 | 16% | |||
Farxiga/Onglyza | AstraZeneca | Diabetes | 8 | — | n/a | |||
Prevymis | Merck & Co. | Infectious disease | 8 | — | n/a | |||
Crysvita | Ultragenyx, Kyowa Kirin | Rare disease | 3 | — | n/a | |||
Erleada | Johnson & Johnson | Cancer | 3 | 1 | 140% | |||
Emgality | Eli Lilly | Neurology | 3 | 1 | 91% | |||
IDHIFA | Bristol Myers Squibb | Cancer | 3 | — | n/a | |||
Tazverik | Epizyme | Cancer | 0 | — | n/a | |||
Nurtec ODT | Biohaven | Neurology | 0 | — | n/a | |||
Trodelvy | Gilead | Cancer | 2 | — | n/a | |||
Evrysdi | Roche | Rare disease | 0 | — | n/a | |||
Lyrica | Pfizer | Neurology | 5 | 31 | (83)% | |||
Letairis | Gilead | Cardiology | 9 | 22 | (59)% | |||
Other Products(4) | 46 | 67 | (31)% | |||||
Total Royalty Receipts | 627 | 576 | 9% | |||||
Distributions to non-controlling interest | (143) | (131) | 9% | |||||
Adjusted Cash Receipts (non-GAAP)(1) | 484 | 446 | 9% |
Amounts shown in the table may not add due to rounding.
Net cash provided by operating activities was
Total Royalty Receipts were
Drivers of royalty receipts in the fourth quarter of 2020 and full year of 2020 are discussed below, based on commentary from the marketers of the products underlying the royalties in the preceding quarter (as royalty receipts generally lag product performance by one calendar quarter).
- Cystic fibrosis franchise – Royalty receipts from Vertex’s cystic fibrosis (CF) franchise, which includes Kalydeco, Orkambi, Symdeko/Symkevi and Trikafta/Kaftrio, all approved for patients with certain mutations causing cystic fibrosis, were $159 million in the fourth quarter of 2020, an increase of 37% compared to the same period of 2019 and
$551 million for 2020, up 30% compared to 2019, primarily driven by the highly successful launch of Trikafta inthe United States .
- Tysabri – Royalty receipts from Tysabri, which is marketed by Biogen for the treatment of multiple sclerosis, were
$93 million in the fourth quarter of 2020, an increase of 10% compared to the same period of 2019. Royalty receipts from Tysabri were$346 million for 2020, an increase of 4% compared to 2019. The increase was driven by demand for Tysabri in the growing high-efficacy segment of the market.
- Imbruvica – Royalty receipts from Imbruvica, which is marketed by AbbVie and Johnson & Johnson for the treatment of blood cancers and chronic graft versus host disease, were
$85 million in the fourth quarter of 2020, an increase of 12% driven by continued penetration in patients with chronic lymphocytic leukemia. Royalty receipts from Imbruvica were$322 million in 2020, an increase of 19% compared to 2019.
- HIV franchise – Royalty receipts from the HIV franchise, which is based on products marketed by Gilead that contain emtricitabine, including Biktarvy, Genvoya and Truvada, among others, were
$78 million in the fourth quarter of 2020, an increase of 10% compared to the same period of 2019. Royalty receipts for the HIV franchise were$294 million for 2020, an increase of 12% compared to 2019. The fourth quarter of 2020 and full year increase was driven by strong performance of Biktarvy offset by decreases in sales of other combination products.
- Januvia, Janumet, Other DPP-IVs – Royalty receipts from the DPP-IVs for type 2 diabetes, which include Januvia and Janumet, both marketed by Merck & Co., were
$40 million in the fourth quarter of 2020, an increase of 11% compared to the same period of 2019. Royalty receipts from the DPP-IVs for 2020 were relatively consistent with 2019.
- Xtandi – Royalty receipts from Xtandi, which is marketed by Pfizer and Astellas for the treatment of prostate cancer, were
$39 million in the fourth quarter of 2020, an increase of 16% compared to the same period of 2019, driven by demand across various prostate cancer indications. Royalty receipts from Xtandi were$146 million for 2020, an increase of 22% compared to 2019.
- Promacta – Royalty receipts from Promacta, which is marketed by Novartis for the treatment of chronic immune thrombocytopenia purpura (ITP) and aplastic anemia, were
$42 million in the fourth quarter of 2020, an increase of 16% compared to the same period of 2019. Global growth was driven by increased use in ITP and further uptake as first-line treatment for severe aplastic anemia inthe United States . Royalty receipts from Promacta were$144 million for 2020, an increase of 67% compared to 2019. We acquired the Promacta royalty inMarch 2019 and did not record royalty receipts for Promacta until the second quarter of 2019.
Distributions to non-controlling interest, which reduce royalty receipts to arrive at Adjusted Cash Receipts, were
Adjusted Cash Receipts(1) were
Adjusted EBITDA(5) is comprised of Adjusted Cash Receipts less payments for operating and professional costs. In the fourth quarter of 2020, Adjusted EBITDA was $434 million, a 5% increase compared to Adjusted EBITDA of
- The increase was largely attributable to the 9% growth in Adjusted Cash Receipts in the fourth quarter of 2020 as compared to the same period in 2019.
- Payments for operating and professional costs amounted to
$50 million in the fourth quarter of 2020 (representing 10% of Adjusted Cash Receipts) as compared to$32 million (representing 7% of Adjusted Cash Receipts) in the same period of 2019 on a pro forma basis, with the increase primarily driven by increased payments for fees related to the initial public offering (IPO) and other operating costs.
Adjusted EBITDA was
Adjusted Cash Flow(2) is comprised of Adjusted EBITDA less ongoing development-stage funding payments, net interest paid and miscellaneous other items. In the fourth quarter of 2020, Adjusted Cash Flow was $423 million, a 22% increase compared to Adjusted Cash Flow of $347 million for the same period of 2019 on a pro forma basis. The increase primarily resulted from the growth in Adjusted Cash Receipts as well as lower net interest paid and lower ongoing development-stage funding payments. Items in the period included:
- Ongoing development-stage funding payments of $2 million in the fourth quarter of 2020 were significantly lower than the $16 million in the same period of 2019, as certain R&D programs (primarily related to the Phase 3 adjuvant studies of Ibrance) reached completion at the end of 2019. Ongoing development-stage funding payments of $20 million during 2020 were significantly lower than the $83 million in 2019.
- Net interest paid of
$1 million in the fourth quarter of 2020 was lower than the$50 million paid in the same period of 2019 on a pro forma basis due to the impact of debt refinancings during 2020 and a shift to semi-annual interest payments with the issuance of$6 billion of senior unsecured notes. Net interest paid of$95 million in 2020 was lower than the$215 million paid in 2019 on a pro forma basis.
Adjusted Cash Flow was
A more comprehensive discussion of the non-GAAP measures utilized by
Key Developments Relating to the Portfolio
The key developments related to
- Cystic fibrosis franchise: In
January 2021 , Vertex Pharmaceuticals announced that theU.S. FDA accepted its sNDA to expand the use of Trikafta to include children ages 6 through 11 years old who have at least one F508del mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene or a mutation in the CFTR gene that is responsive based on in vitro data. The FDA granted Priority Review of the sNDA and assigned a PDUFA target action date ofJune 8, 2021 .
- Trodelvy: In
December 2020 , Gilead filed Supplemental Biologics License Applications (sBLAs) for Trodelvy with the FDA for full approval for the treatment of patients with metastatic triple-negative breast cancer (mTNBC) who have received at least two prior therapies for metastatic disease and accelerated approval for third line metastatic urothelial cancer (mUC).
- Omecamtiv mecarbil: In
November 2020 , Amgen, Cytokinetics andServier presented the results of GALACTIC-HF study, a Phase 3 trial of omecamtiv mecarbil in patients with heart failure, at the American Heart Association Scientific Sessions. The trial met the primary composite endpoint of reduction in cardiovascular death or heart failure events, but did not meet the secondary endpoint of reduction in cardiovascular death. Cytokinetics subsequently regained global rights to develop and commercialize omecamtiv mecarbil when Amgen andServier elected to terminate their collaboration agreement effective as ofMay 2021 . Following Phase 3 results and the termination of the collaboration,Royalty Pharma recorded a$90 million write-off to the royalty investment given the uncertainty around the future of omecamtiv.
Summary of Recent Royalty Acquisition Activity
- Cystic fibrosis franchise: In
November 2020 ,Royalty Pharma announced that it acquired the residual royalty interest in Vertex's CF franchise owned by theCF Foundation for an upfront payment of$575 million and a potential milestone of$75 million payable under certain circumstances. As part of previous agreements with theCF Foundation ,Royalty Pharma was obligated to pay theCF Foundation 50% of royalties attributable to revenue over$5.8 billion in any calendar year. This obligation was eliminated with this transaction andRoyalty Pharma is entitled to all royalties above the previous revenue threshold.
- Orladeyo and BCX9930: In
December 2020 ,Royalty Pharma announced that it acquired a royalty interest in BioCryst's Orladeyo (berotralstat), an oral therapy to prevent attacks of hereditary angioedema (HAE) in adults and pediatric patients 12 years and older and BCX9930, an oral Factor D inhibitor in development for the treatment of complement-mediated diseases.Royalty Pharma provided BioCryst an upfront cash payment of$125 million and will receive royalties of 8.75% on direct annual net sales of Orladeyo up to$350 million , 2.75% on sales between$350 million and$550 million , no royalty on sales over$550 million , and a tiered percentage of sublicense revenue for Orladeyo in certain territories. In addition,Royalty Pharma will receive a 1.0% royalty on global net sales of BCX9930, if approved.
- Seltorexant: In
January 2021 ,Royalty Pharma announced that it acquired Minerva Neuroscience’s royalty interest in seltorexant for an upfront payment of$60 million and up to$95 million in additional milestone payments. The additional payments to Minerva will be contingent on the achievement of certain clinical, regulatory and commercialization milestones. Seltorexant is currently in Phase 3 development for the treatment of major depressive disorder (MDD) with insomnia symptoms byJanssen Pharmaceutica, N.V. , a subsidiary of Johnson & Johnson.
Liquidity and Capital Resources
- As of
December 31, 2020 ,Royalty Pharma had cash, cash equivalents and marketable securities in the amount of$2.0 billion and$5 .8 billion of long-term debt with principal value of$6.0 billion .
2021 Financial Guidance
Provided |
|
Adjusted Cash Receipts (non-GAAP) excluding new transactions announced after the date of this release |
|
2020 to 2025 Long-Term Outlook
Provided |
Previous outlook | |
Adjusted Cash Receipts (non-GAAP) including new transactions | 7% to 10% CAGR | 6% to 9% CAGR |
Financial Results Call
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About
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Forward-Looking Statements
The information set forth herein does not purport to be complete or to contain all of the information you may desire. Statements contained herein are made as of the date of this document unless stated otherwise, and neither the delivery of this document at any time, nor any sale of securities, shall under any circumstances create an implication that the information contained herein is correct as of any time after such date or that information will be updated or revised to reflect information that subsequently becomes available or changes occurring after the date hereof.
This document contains statements that constitute “forward-looking statements” as that term is defined in
Certain information contained in this document relates to or is based on studies, publications, surveys and other data obtained from third-party sources and the company's own internal estimates and research. While the company believes these third-party sources to be reliable as of the date of this document, it has not independently verified, and makes no representation as to the adequacy, fairness, accuracy or completeness of, any information obtained from third-party sources. In addition, all of the market data included in this document involves a number of assumptions and limitations, and there can be no guarantee as to the accuracy or reliability of such assumptions. Finally, while the company believes its own internal research is reliable, such research has not been verified by any independent source.
For further information, please reference
Use of Non-GAAP Measures
Adjusted Cash Receipts, Adjusted EBITDA and Adjusted Cash Flow are non-GAAP measures presented as supplemental measures to
In addition,
Management believes that Adjusted EBITDA is an important non-GAAP measure in analyzing liquidity and is a key component of certain material covenants contained within the company’s Credit Agreement. Noncompliance with the interest coverage ratio and leverage ratio covenants under the credit agreement could result in lenders requiring the company to immediately repay all amounts borrowed. If
Management uses Adjusted Cash Flow to evaluate its ability to generate cash and performance of the business and to evaluate the company’s performance as compared to its peer group. Management also uses Adjusted Cash Flow to compare its performance against non-GAAP adjusted net income measures used by many companies in the biopharmaceutical industry, even though each company may customize its own calculation and therefore one company’s metric may not be directly comparable to another’s.
The non-GAAP financial measures used in this press release have limitations as analytical tools, and you should not consider them in isolation or as a substitute for the analysis of
Condensed Consolidated Income Statement (unaudited)
Table 1
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($ in millions) | 2020 | 2019 | 2020 | 2019 |
Total income and revenues | ||||
Income from financial royalty assets | 524 | 420 | 1,960 | 1,649 |
Revenue from intangible royalty assets | 40 | 35 | 143 | 146 |
Other royalty income | 7 | 3 | 19 | 20 |
Total income and other revenues | 572 | 457 | 2,122 | 1,814 |
Operating expenses | ||||
Research and development funding expense | 8 | 16 | 26 | 83 |
Provision for changes in expected cash flows from financial royalty assets | 129 | (919) | 231 | (1,019) |
Amortization of intangible royalty assets | 6 | 6 | 23 | 24 |
General and administrative expenses | 50 | 23 | 182 | 103 |
Other operating expenses | 65 | — | 65 | — |
Total operating expenses | 258 | (874) | 527 | (809) |
Operating income | 314 | 1,332 | 1,595 | 2,623 |
Other (income)/expense | ||||
Equity in (earnings)/loss of non-consolidated affiliates | (10) | 11 | (44) | 33 |
Interest expense | 38 | 63 | 157 | 269 |
Other income, net | (80) | (189) | (219) | (139) |
Total other (income)/expense, net | (53) | (115) | (107) | 162 |
Consolidated net income before tax | 367 | 1,447 | 1,702 | 2,461 |
Income tax expense | — | — | — | — |
Consolidated net income | 367 | 1,447 | 1,702 | 2,461 |
Less: Net income attributable to non-controlling interest | (196) | (26) | (727) | (113) |
Net income attributable to controlling interest | 171 | 1,420 | 975 | 2,349 |
Amounts may not add due to rounding.
Selected Balance Sheet Data (unaudited)
Table 2
($ in millions) | As of |
As of |
||
Cash and cash equivalents | 1,009 | 246 | ||
Marketable securities | 983 | 94 | ||
Total financial royalty assets, net | 12,955 | 11,295 | ||
Total assets | 16,020 | 12,450 | ||
Current portion of long-term debt | — | 282 | ||
Long-term debt, excluding current portion | 5,817 | 5,956 | ||
Total liabilities | 6,124 | 6,308 | ||
Total shareholders’ equity | 9,896 | 6,141 | ||
Condensed Consolidated Statements of Cash Flows (unaudited)
Table 3
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|||
($ in millions) | 2020 | 2019 | 2020 | 2019 |
Cash flows from operating activities: | ||||
Cash collections from financial royalty assets | 573 | 532 | 2,122 | 1,934 |
Cash collections from intangible royalty assets | 40 | 36 | 144 | 143 |
Other royalty cash collections | 6 | 3 | 18 | 27 |
Distributions from non-consolidated affiliates | 6 | — | 42 | 14 |
Interest received | 0 | 2 | 8 | 20 |
Swap collateral received | — | — | 45 | 0 |
Swap collateral posted | — | — | — | (46) |
Swap termination payments | — | — | (35) | — |
Ongoing development-stage funding payments | (2) | (16) | (20) | (83) |
Upfront development-stage funding payments | (6) | — | (6) | — |
Payments for operating and professional costs | (50) | (18) | (180) | (89) |
Interest paid | (1) | (60) | (103) | (255) |
Net cash provided by operating activities | 566 | 478 | 2,035 | 1,667 |
Cash flows from investing activities: | ||||
Distributions from non-consolidated affiliates | — | — | 15 | — |
Purchases of available for sale debt securities | — | — | — | (125) |
Purchase of warrants | — | (9) | — | (9) |
Purchase of equity securities | — | (79) | (50) | (79) |
Purchase of marketable securities | (610) | (67) | (1,705) | (817) |
Proceeds from available for sale debt securities | 3 | — | 3 | 150 |
Proceeds from sales and maturities of marketable securities | 206 | 564 | 815 | 725 |
Proceeds from equity securities | 385 | — | 385 | — |
Investments in non-consolidated affiliates | (11) | (4) | (40) | (27) |
Acquisitions of financial royalty assets | (805) | (467) | (2,182) | (1,721) |
Milestone payments | — | — | — | (250) |
Net cash used in investing activities | (832) | (63) | (2,759) | (2,154) |
Cash flows from financing activities: | ||||
Distributions to shareholders/unitholders | — | (175) | (285) | (739) |
Distributions to non-controlling interest | (143) | (37) | (544) | (154) |
Distributions to non-controlling interest – other | (107) | — | (181) | — |
Dividends to shareholders | (58) | — | (112) | — |
Contributions from non-controlling interest- R&D | 2 | — | 8 | — |
Contributions from non-controlling interest- other | 29 | — | 59 | — |
Scheduled repayments of long-term debt | — | (74) | (94) | (294) |
Repayments of long-term debt | — | — | (11,116) | — |
Proceeds from issuance of long-term debt | — | — | 11,891 | — |
Debt issuance costs and other | 0 | — | (47) | — |
Purchase of treasury interests | — | — | — | (4) |
Proceeds from issuance of Class A ordinary shares upon IPO, net of offering costs | (1) | — | 1,909 | — |
Net cash (used in)/provided by financing activities | (277) | (286) | 1,487 | (1,192) |
Net change in cash and cash equivalents | (544) | 130 | 762 | (1,678) |
Cash and cash equivalents, beginning of period | 1,553 | 116 | 246 | 1,924 |
Cash and cash equivalents, end of period | 1,009 | 246 | 1,009 | 246 |
Amounts may not add due to rounding.
Non-GAAP Financial Measures (unaudited)
Table 4
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|||||||
($ in millions) | 2020 | 2019 Pro Forma(3) |
change | 2020 | 2019 Pro Forma(3) |
change | ||
Net cash provided by operating activities (GAAP) | 566 | 478 | 18% | 2,035 | 1,673 | 22% | ||
Products: | ||||||||
Cystic fibrosis franchise | 159 | 116 | 37% | 551 | 425 | 30% | ||
Tysabri | 93 | 85 | 10% | 346 | 333 | 4% | ||
Imbruvica | 85 | 76 | 12% | 322 | 271 | 19% | ||
HIV franchise | 78 | 71 | 10% | 294 | 263 | 12% | ||
Januvia, Janumet, Other DPP-IVs | 40 | 36 | 11% | 144 | 143 | 0% | ||
Xtandi | 39 | 34 | 16% | 146 | 120 | 22% | ||
Promacta | 42 | 36 | 16% | 144 | 86 | 67% | ||
Farxiga/Onglyza | 8 | — | n/a | 25 | — | n/a | ||
Prevymis | 8 | — | n/a | 21 | — | n/a | ||
Crysvita | 3 | — | n/a | 9 | — | n/a | ||
Erleada | 3 | 1 | 140% | 8 | 3 | 194% | ||
Emgality | 3 | 1 | 91% | 10 | 2 | 291% | ||
IDHIFA | 3 | — | n/a | 6 | — | n/a | ||
Tazverik | 0 | — | n/a | 1 | — | n/a | ||
Nurtec ODT | 0 | — | n/a | 1 | — | n/a | ||
Trodelvy | 2 | — | n/a | 3 | — | n/a | ||
Evrysdi | 0 | — | n/a | 0 | — | n/a | ||
Lyrica | 5 | 31 | (83)% | 23 | 128 | (82)% | ||
Letairis | 9 | 22 | (59)% | 40 | 113 | (64)% | ||
Other Products(4) | 46 | 67 | (31)% | 250 | 415 | (40)% | ||
Total Royalty Receipts | 627 | 576 | 9% | 2,344 | 2,302 | 2% | ||
Distributions to non-controlling interest | (143) | (131) | 9% | (544) | (526) | 3% | ||
Adjusted Cash Receipts (non-GAAP)(1) | 484 | 446 | 9% | 1,800 | 1,776 | 1% | ||
Payments for operating and professional costs | (50) | (32) | 57% | (180) | (145) | 24% | ||
Adjusted EBITDA (non-GAAP)(5) | 434 | 413 | 5% | 1,621 | 1,631 | (1)% | ||
Ongoing development-stage funding payments | (2) | (16) | (88)% | (20) | (83) | (75)% | ||
Interest paid, net | (1) | (50) | (99)% | (95) | (215) | (55)% | ||
Swap termination payments | — | — | n/a | (35) | (35) | 0% | ||
Swap collateral received | — | — | n/a | 45 | — | n/a | ||
Investment in non-consolidated affiliates | (11) | (4) | 150% | (40) | (27) | 48% | ||
Contributions from non-controlling interest- R&D | 2 | 4 | (36)% | 8 | 19 | (56)% | ||
Adjusted Cash Flow (non-GAAP)(2) | 423 | 347 | 22% | 1,483 | 1,290 | 15% | ||
Amounts may not add due to rounding. | ||||||||
GAAP to Non-GAAP Reconciliation (unaudited)
Table 5
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|||
($ in millions) | 2020 | 2019 Pro Forma(3) |
2020 | 2019 Pro Forma(3) |
Net cash provided by operating activities (GAAP) | 566 | 478 | 2,035 | 1,673 |
Adjustments: | ||||
Proceeds from available for sale debt securities(6) | 3 | — | 3 | 150 |
Distributions from non-consolidated affiliates – investing(7) | — | — | 15 | — |
Interest paid, net(7) | 1 | 50 | 95 | 215 |
Ongoing development-stage funding payments(8) | 2 | 16 | 20 | 83 |
Upfront development-stage funding payments(8) | 6 | — | 6 | — |
Payments for operating and professional costs | 50 | 32 | 180 | 145 |
Swap termination payments | — | — | 35 | 35 |
Distributions to non-controlling interest(7) | (143) | (131) | (544) | (526) |
Swap collateral received, net(7) | — | — | (45) | — |
Adjusted Cash Receipts (non-GAAP)(1) | 484 | 446 | 1,800 | 1,776 |
Net cash provided by operating activities (GAAP) | 566 | 478 | 2,035 | 1,673 |
Adjustments: | ||||
Proceeds from available for sale debt securities(6) | 3 | — | 3 | 150 |
Distributions from non-consolidated affiliates – investing(7) | — | — | 15 | — |
Interest paid, net(7) | 1 | 50 | 95 | 215 |
Ongoing development-stage funding payments(8) | 2 | 16 | 20 | 83 |
Upfront development-stage funding payments(8) | 6 | — | 6 | — |
Swap termination payments | — | — | 35 | 35 |
Distributions to non-controlling interest(7) | (143) | (131) | (544) | (526) |
Swap collateral received, net(7) | — | — | (45) | — |
Adjusted EBITDA (non-GAAP)(5) | 434 | 413 | 1,621 | 1,631 |
Net cash provided by operating activities (GAAP) | 566 | 478 | 2,035 | 1,673 |
Adjustments: | ||||
Proceeds from available for sale debt securities(6) | 3 | — | 3 | 150 |
Distributions from non-consolidated affiliates – investing(7) | — | — | 15 | — |
Upfront development-stage funding payments(8) | 6 | — | 6 | — |
Contribution from non-controlling interest- R&D(7) | 2 | 4 | 8 | 19 |
Distributions to non-controlling interest(7) | (143) | (131) | (544) | (526) |
Investment in non-consolidated affiliates(7)(9) | (11) | (4) | (40) | (27) |
Adjusted Cash Flow (non-GAAP)(2) | 423 | 347 | 1,483 | 1,290 |
Amounts may not add due to rounding.
Notes
(1) Adjusted Cash Receipts is a measure calculated with inputs directly from the Statement of Cash Flows and includes (1) royalty receipts: (i) cash collections from royalty assets (financial assets and intangible assets), (ii) other royalty cash collections, (iii) distributions from non-consolidated affiliates, plus (2) proceeds from available for sale debt securities (primarily Tecfidera milestone payments in 2019), and less (3) distributions to non-controlling interest, which represents distributions to historical non-controlling interest attributable to a de minimis interest in RPCT held by certain legacy investors and to a new non-controlling interest that was created as a result of the Exchange Offer Transactions in
(2) Adjusted Cash Flow is defined as Adjusted EBITDA less (1) ongoing development-stage funding payments, (2) interest paid, net, (3) swap collateral (posted) or received, net, (4) swap termination payments and (5) investment in non-consolidated affiliates, and plus (1) contributions from non-controlling interest – R&D, all directly reconcilable to the Statement of Cash Flows. See GAAP to Non-GAAP reconciliation at Table 5.
(3) To aid in comparability, three and twelve months ended
(4) Other Products include royalties on the following products: Bosulif (a product co-developed by
(5) Adjusted EBITDA is important to lenders and is defined under the credit agreement as Adjusted Cash Receipts less payments for operating and professional costs. Operating and professional costs are comprised of payments for operating and professional costs and payments for rebates from the Statement of Cash Flows. See GAAP to Non-GAAP reconciliation at Table 5.
(6) Receipts from our Tecfidera milestone payments are presented as Proceeds from available for sale debt securities on the Statement of Cash Flows. In 2020, amount includes a payment from Biohaven in respect of an expired option to exercise additional funding of the Biohaven Series A Preferred Shares.
(7) The table below shows the line item for each adjustment and the direct location for such line item on the Statement of Cash Flows.
Reconciling adjustment | Statement of Cash Flows classification |
Investments in non-consolidated affiliates | Investing activities |
Distributions to non-controlling interest | Financing activities |
Interest paid, net | Operating activities (Interest paid less interest received) |
Swap collateral received, net | Operating activities (Swap collateral received less swap collateral posted) |
Distributions from non-consolidated affiliates - investing | Investing activities |
Contributions from non-controlling interest- R&D | Financing activities |
(8) Lenders consider all payments made to support R&D activities for products undergoing late-stage development similar to asset acquisitions as these funds are expected to generate operational returns in the future. All ongoing and upfront development-stage funding payments run through R&D funding expense in net income and are added back in aggregate to net cash provided by operating activities to arrive at Adjusted EBITDA. As a result, Adjusted EBITDA captures the full add-back for R&D funding payments, while Adjusted Cash Flow only reflects the add-back for the upfront portion of development-stage funding payments due to the fact that ongoing development-stage funding payments are considered an ongoing business expense.
(9)
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Source: RP Management, LLC