Bristol Myers Squibb Reports Fourth Quarter and Full-Year Financial Results for 2023

Bristol Myers Squibb Reports Fourth Quarter and Full-Year Financial Results for 2023




Bristol Myers Squibb Reports Fourth Quarter and Full-Year Financial Results for 2023

Results Reflect Continued Strength of In-Line and New Products, Pipeline Execution and Business Development Activity, Supporting Growth Momentum into 2024  

  • Reports Fourth Quarter Revenues of $11.5 Billion; GAAP EPS of $0.87 and Non-GAAP EPS of $1.70

    • In-Line and New Product Portfolio Revenues Increased 9% to $9.8 Billion
  • Reports Full-Year Revenues of $45.0 Billion; GAAP EPS of $3.86 and Non-GAAP EPS of $7.51

    • In-Line and New Product Portfolio Revenues Increased 7% to $37.9 Billion
  • Strengthens Long-Term Growth Profile Through Multiple Transactions, Including Planned Acquisitions of Karuna Therapeutics and RayzeBio and Strategic Collaboration with SystImmune; Completes Purchase of Mirati Therapeutics
  • Advances Research Pipeline Including U.S. Approval of Augtyro and FDA Acceptance of sBLAs for Breyanzi in Follicular Lymphoma and Mantle Cell Lymphoma for Priority Review
  • Provides 2024 Guidance with Revenues Increasing by Low Single-Digits; Non-GAAP EPS Range $7.10 to $7.40, Excludes Impact of Pending Transactions

PRINCETON, N.J.–(BUSINESS WIRE)–Bristol Myers Squibb (NYSE: BMY) today reports results for the fourth quarter and full year of 2023, which reflect strong pipeline acceleration, continued portfolio diversification, and momentum in our business.


We saw good performance in the fourth quarter from our in-line and new products and took several actions to strengthen the company and build a foundation for sustainable growth,” said Christopher Boerner, Ph.D., chief executive officer, Bristol Myers Squibb. “In 2024, our focus is on delivering strong commercial execution and accelerating opportunities that enhance our growth profile in the middle of the decade and beyond.”

 

Fourth Quarter

 

Full Year

$ in millions, except per share amounts

2023

 

2022

 

Change

 

Change Excl.

F/X**

 

2023

 

2022

 

Change

 

Change Excl.

F/X**

Total Revenues

$11,477

 

$11,406

 

1%

 

1%

 

$45,006

 

$46,159

 

(2)%

 

(2)%

EPS — GAAP*

0.87

 

0.95

 

(8)%

 

N/A

 

3.86

 

2.95

 

31%

 

N/A

EPS — Non-GAAP*

1.70

 

1.82

 

(7)%

 

N/A

 

7.51

 

7.70

 

(2)%

 

N/A

Acquired IPRD charge and Licensing Income Net Impact (Decrease)/Increase

(0.20)

 

(0.01)

 

N/A

 

N/A

 

(0.28)

 

(0.24)

 

N/A

 

N/A

* GAAP and Non-GAAP earnings per share include the net impact of Acquired IPRD charges and licensing income.

** See “Use of Non-GAAP Financial Information”.

FOURTH QUARTER RESULTS

All comparisons are made versus the same period in 2022 unless otherwise stated.

  • Bristol Myers Squibb posted fourth quarter revenues of $11.5 billion, an increase of 1% both on a reported and when adjusted for foreign exchange basis, primarily due to higher sales of new product portfolio, as well as Eliquis and Opdivo, partially offset by lower sales of Revlimid.
  • U.S. revenues increased 1% to $8.0 billion primarily due to higher sales of new product portfolio, Eliquis and Opdivo, partially offset by lower sales of Revlimid.
  • International revenues remained relatively flat at $3.5 billion, primarily due to lower sales of Revlimid, offset by higher sales of new product portfolio and Opdivo.
  • On a GAAP basis, gross margin decreased from 77.3% to 76.1% and on a non-GAAP basis, gross margin decreased from 77.9% to 76.4% primarily due to product mix and lower hedge settlement gains.
  • On a GAAP and non-GAAP basis, marketing, selling and administrative expenses decreased 9% to $2.1 billion primarily due to timing of spend.
  • On a GAAP and non-GAAP basis, research and development expenses remained relatively flat at $2.5 billion.
  • On a GAAP and non-GAAP basis, Acquired IPRD increased to $600 million from $52 million primarily due to the reacquired mavacamten rights of $445 million in China and certain other Asian territories. On a GAAP and non-GAAP basis, licensing income was $67 million compared to $16 million during the same period a year ago.
  • On a GAAP basis, amortization of acquired intangible assets decreased 3% to $2.3 billion primarily due to the Abraxane marketed product right being fully amortized in the fourth quarter of 2022.
  • On a GAAP basis, income tax benefit was $88 million despite pre-tax earnings of $1.7 billion primarily due to a valuation allowance reversal related to unrealized equity investment losses and foreign currency. In 2022, the income tax benefit was $166 million despite pre-tax earnings of $1.9 billion primarily due to the release of income tax reserves. On a non-GAAP basis, the effective tax rate changed from 10.9% to 14.9%, primarily due to release of income tax reserves in 2022.
  • The company reported on a GAAP basis net earnings attributable to Bristol Myers Squibb of $1.8 billion, or $0.87 per share, compared to $2.0 billion, or $0.95 per share, for the same period a year ago. In addition to the items above, the decrease in GAAP EPS was driven by lower losses in equity investments. The company reported on a non-GAAP basis net earnings attributable to Bristol Myers Squibb of $3.5 billion, or $1.70 per share, compared to $3.9 billion, or $1.82 per share, for the same period a year ago. The EPS results in the fourth quarter of 2023 also include the impact of lower weighted-average common shares outstanding.

FOURTH QUARTER PRODUCT REVENUE HIGHLIGHTS

($ amounts in millions)

 

Quarter Ended December

31, 2023

 

% Change from Quarter

Ended December 31,

2022

 

% Change from

Quarter Ended

December 31,

2022 Ex-F/X**

 

 

U.S.(c)

 

Int’l

 

WW(d)

 

U.S.(c)

 

Int’l

 

WW(d)

 

Int’l

 

WW(d)

In-Line Products

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Eliquis

 

$

1,899

 

$

975

 

$

2,874

 

11%

 

1%

 

7%

 

(3)%

 

6%

Opdivo

 

 

1,411

 

 

976

 

 

2,387

 

12%

 

3%

 

8%

 

4%

 

8%

Orencia

 

 

766

 

 

219

 

 

985

 

8%

 

8%

 

8%

 

11%

 

9%

Pomalyst/Imnovid

 

 

632

 

 

258

 

 

890

 

1%

 

2%

 

1%

 

—%

 

1%

Yervoy

 

 

343

 

 

223

 

 

566

 

(1)%

 

—%

 

— %

 

1%

 

—%

Sprycel

 

 

417

 

 

109

 

 

526

 

—%

 

(32)%

 

(9)%

 

(31)%

 

(9)%

Mature and other products (a)

 

 

202

 

 

278

 

 

480

 

9%

 

(6)%

 

—%

 

(5)%

 

1%

Total In-Line Products

 

 

5,670

 

 

3,038

 

 

8,708

 

8%

 

(1) %

 

5 %

 

(1)%

 

5%

New Product Portfolio

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Reblozyl

 

 

274

 

 

46

 

 

320

 

75%

 

10%

 

61%

 

5%

 

60%

Opdualag

 

 

187

 

 

3

 

 

190

 

80%

 

N/A

 

83%

 

N/A

 

83%

Abecma

 

 

56

 

 

44

 

 

100

 

(40)%

 

42%

 

(20)%

 

39%

 

(21)%

Zeposia

 

 

101

 

 

32

 

 

133

 

74%

 

52%

 

68%

 

43%

 

66%

Breyanzi

 

 

85

 

 

16

 

 

101

 

*

 

23%

 

84%

 

23%

 

84%

Camzyos

 

 

84

 

 

4

 

 

88

 

*

 

N/A

 

*

 

N/A

 

*

Sotyktu

 

 

56

 

 

7

 

 

63

 

*

 

N/A

 

*

 

N/A

 

*

Onureg

 

 

31

 

 

16

 

 

47

 

15%

 

60%

 

27%

 

50%

 

24%

Inrebic

 

 

19

 

 

10

 

 

29

 

12%

 

67%

 

26%

 

67%

 

26%

Augtyro

 

 

1

 

 

 

 

1

 

N/A

 

N/A

 

N/A

 

N/A

 

N/A

Total New Product Portfolio

 

 

894

 

 

178

 

 

1,072

 

71%

 

45%

 

66%

 

39%

 

65%

Total In-Line and New Product Portfolio

 

 

6,564

 

 

3,216

 

 

9,780

 

13%

 

1%

 

9%

 

1%

 

9%

Recent LOE Products (b)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Revlimid

 

 

1,262

 

 

188

 

 

1,450

 

(38)%

 

(21)%

 

(36)%

 

(20)%

 

(36)%

Abraxane

 

 

177

 

 

70

 

 

247

 

53%

 

11%

 

38%

 

22%

 

42%

Total Recent LOE Products

 

 

1,439

 

 

258

 

 

1,697

 

(33)%

 

(15)%

 

(30)%

 

(11)%

 

(30)%

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Total Revenues

 

$

8,003

 

$

3,474

 

$

11,477

 

1%

 

—%

 

1%

 

—%

 

1%

*

In excess of +100%

**

See “Use of Non-GAAP Financial Information”.

(a)

Includes over-the-counter (OTC) products, royalty revenue and mature products.

(b)

Recent LOE Products includes products with significant expected decline in revenue from a prior reporting period as a result of a loss of exclusivity.

(c)

Includes Puerto Rico.

(d)

Worldwide (WW) includes U.S. and International (Int’l).

FOURTH QUARTER PRODUCT REVENUE HIGHLIGHTS

In-Line Products

Revenues for in-line products in the fourth quarter were $8.7 billion compared to $8.3 billion in the prior year period. In-line products revenue was largely driven by:

  • Eliquis worldwide revenues increased 7%, or 6% when adjusted for foreign exchange impacts. U.S. revenues were $1.9 billion compared to $1.7 billion in the prior year period, representing an increase of 11% primarily due to higher demand, partially offset by GTN adjustments in 2023. International revenues were $975 million compared to $970 million in the prior year period, representing an increase of 1%, or a decrease of 3% when adjusted for foreign exchange impacts, primarily driven by lower average net selling prices and generic erosion in several European countries.
  • Opdivo worldwide revenues increased 8% both on a reported and when adjusted for foreign exchange basis. U.S. revenues increased 12% to $1.4 billion compared to $1.3 billion in the prior year period primarily due to higher demand. International revenues were $976 million compared to $951 million in the prior year period, representing an increase of 3%, or 4% when adjusted for foreign exchange impacts, primarily due to higher demand as a result of launches for new indications and core indications.

New Product Portfolio

  • New product portfolio worldwide revenues increased to $1.1 billion compared to $645 million in the prior year period, representing a growth of 66%, or 65% when adjusted for foreign exchange impacts, primarily driven by higher demand across the portfolio, including for Reblozyl, Opdualag, Camzyos, Sotyktu, Zeposia and Breyanzi.

Recent LOE Products

  • Revlimid worldwide revenues declined to $1.5 billion compared to $2.3 billion in the prior year period, representing a decline of 36%, both on a reported and when adjusted for foreign exchange basis, primarily due to generic erosion.

PRODUCT AND PIPELINE UPDATE

The company recently achieved several important regulatory and clinical milestones. In November 2023, Augtyro received U.S. regulatory approval in non-small cell lung cancer. The U.S. Food and Drug Administration (FDA) also accepted supplemental Biologics License Applications (sBLAs) for Breyanzi to expand into follicular lymphoma and mantle cell lymphoma.

Oncology

Category

Asset

Milestone

Regulatory

KRAZATI®

(adagrasib)

The European Commission (EC) granted conditional marketing authorization for KRAZATI as a targeted treatment option for adult patients with KRASG12C -mutated advanced non-small cell lung cancer (NSCLC) and disease progression after at least one prior systemic therapy.

 

repotrectinib

The European Medicines Agency (EMA) validated the marketing authorization application for repotrectinib as a treatment for ROS1 tyrosine kinase inhibitor (TKI)-naïve and -pretreated adult patients with ROS1-positive locally advanced or metastatic NSCLC and TKI naïve- and -pretreated adult and pediatric patients 12 years and older with NTRK-positive locally advanced or metastatic solid tumors. The application was based on the registrational Phase 1/2 TRIDENT-1 trial and CARE study. Application validation confirms the submission is complete and begins the EMA’s centralized review procedure.

 

Opdivo®

(nivolumab)

The FDA accepted the sBLA for Opdivo in combination with cisplatin-based chemotherapy as a first-line treatment for adult patients with unresectable or metastatic urothelial carcinoma. The FDA granted the application Priority Review and assigned a Prescription Drug User Fee Act (PDUFA) goal date of April 5, 2024.

 

In addition, the EMA validated the type II variation application for Opdivo in combination with cisplatin-based chemotherapy as a first-line treatment for adult patients with unresectable or metastatic urothelial carcinoma. Application validation confirms the submission is complete and begins the EMA’s centralized review procedure.

 

The FDA’s sBLA acceptance and the EMA’s application validation are based on results from the Phase 3 CheckMate -901 trial. 

 

AugtyroTM

(repotrectinib)

The FDA approved Augtyro, a TKI, for the treatment of adult patients with locally advanced or metastatic ROS1-positive NSCLC. The approval is based on results from the pivotal TRIDENT-1 study.

Clinical &

Research

Subcutaneous

nivolumab

Data from the Phase 3 CheckMate -67T trial, evaluating the subcutaneous formulation of Opdivo (nivolumab) co-formulated with Halozyme’s proprietary recombinant human hyaluronidase compared to intravenous Opdivo in patients with advanced or metastatic clear cell renal cell carcinoma who have received prior systemic therapy, demonstrated noninferiority for the co-primary endpoints of Cavgd28 (time-averaged Opdivo serum concentration over 28 days) and Cminss (trough serum concentration at steady state) compared to intravenous Opdivo. In addition, subcutaneous nivolumab displayed noninferior objective response rate as assessed by Blinded Independent Central Review (BICR) versus intravenous Opdivo.

 

Opdivo

Four-year follow-up results from the CheckMate -9ER trial evaluating Opdivo in combination with CABOMETYX® (cabozantinib) vs. sunitinib in patients with previously untreated advanced or metastatic renal cell carcinoma (RCC) continued to show superior progression-free survival (PFS) and objective response rates in patients treated with Opdivo plus CABOMETYX over sunitinib, regardless of risk classification based on International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) scores. Superior overall survival (OS) was also observed in patients treated with the combination. 

 

Opdivo+Yervoy

Eight-year data from the Phase 3 CheckMate -214 trial evaluating Opdivo plus Yervoy versus sunitinib continued to demonstrate long-term survival results, reducing the risk of death by 28% in patients with previously untreated advanced or metastatic RCC, regardless of IMDC risk group. Patients treated with Opdivo plus Yervoy maintained superior survival and more durable response benefits compared to those who received sunitinib in both patients with intermediate- and poor-risk prognostic factors and across all randomized patients.

 

 

The Phase 3 CheckMate -8HW trial evaluating Opdivo plus Yervoy compared to investigator’s choice of chemotherapy as a first-line treatment for patients with microsatellite instability-high or mismatch repair deficient metastatic colorectal cancer (MSI-H/dMMR mCRC) met the dual primary endpoint of PFS as assessed by BICR at a pre-specified interim analysis. The study is ongoing to assess the other dual primary endpoint of PFS per BICR in patients receiving Opdivo plus Yervoy compared to Opdivo alone, as well as secondary endpoints, including overall survival.

 

In addition, data from the Phase 3 CheckMate -8HW trial showed that the combination of Opdivo plus Yervoy reduced the risk of disease progression or death by 79% versus chemotherapy as a first-line treatment for patients with MSI-H/dMMR mCRC compared to chemotherapy. Opdivo plus Yervoy is the first dual immunotherapy regimen to demonstrate significant efficacy benefit compared to chemotherapy in MSI-H/dMMR mCRC.

 

OpdualagTM

(nivolumab and

relatlimab)

The Phase 3 RELATIVITY-123 trial evaluating the fixed-dose combination of nivolumab and relatlimab for the treatment of microsatellite stable metastatic colorectal cancer patients whose disease has progressed following at least one, but no more than four, prior lines of therapy for metastatic disease will be discontinued due to futility based on a planned analysis conducted by an independent data monitoring committee. It was determined that the trial was unlikely to meet its primary endpoints upon completion. The recommendation to stop the study was not based on safety concerns.

Hematology

Category

Asset

Milestone

Regulatory

Abecma®

(idecabtagene

vicleucel)

The Committee for Medicinal Products for Human Use (CHMP) of the EMA has recommended marketing authorization approval of Abecma for the treatment of adult patients with relapsed and refractory multiple myeloma who have received at least two prior therapies, including an immunomodulatory agent, a proteasome inhibitor, and an anti-CD38 monoclonal antibody. The CHMP recommendation will now be reviewed by the EC, which has the authority to approve medicines for the European Union.

 

Reblozyl®

(luspatercept-

aamt)

Japan’s Ministry of Health, Labour and Welfare (MHLW) granted manufacturing and marketing approval for Reblozyl 25 mg/75 mg injection for subcutaneous use indicated for myelodysplastic syndrome (MDS)-related anemia. The approval is based on the results of the global Phase 3 COMMANDS trial and the Phase 3 MEDALIST study, as well as a Japanese Phase 2 study (Study MDS-003) in red blood cell transfusion-independent low-risk MDS patients.

 

Breyanzi®

(lisocabtagene

maraleucel)

The FDA accepted sBLAs for Breyanzi to expand into new indications to include the treatment of adult patients with relapsed or refractory follicular lymphoma (FL) and relapsed or refractory mantle cell lymphoma (MCL) after a Bruton tyrosine kinase inhibitor. The FDA granted both applications Priority Review and assigned a PDUFA goal date of May 23, 2024, for Breyanzi in relapsed or refractory FL and May 31, 2024, for Breyanzi in relapsed or refractory MCL.

 

In addition, Japan’s MHLW has also accepted the company’s supplemental New Drug Application (sNDA) for Breyanzi for the treatment of relapsed or refractory FL.

 

In relapsed or refractory FL, the applications for Breyanzi in the U.S. and Japan are based on results from the TRANSCEND FL study. In relapsed or refractory MCL, the application for Breyanzi in the U.S. is based on results from the MCL cohort of the TRANSCEND NHL 001 study.

 

Abecma

Japan’s MHLW granted manufacturing and marketing approval of the sNDA for an additional indication for Abecma for patients with relapsed or refractory multiple myeloma who have received at least two prior therapies, including an immunomodulatory agent, a proteasome inhibitor, and an anti-CD38 antibody. The approval is based on the interim analysis from the KarMMa-3 trial.

 

Breyanzi

The FDA accepted the sBLA for Breyanzi to expand its current indication to include the treatment of adult patients with relapsed or refractory chronic lymphocytic leukemia or small lymphocytic lymphoma who received a prior Bruton tyrosine kinase inhibitor and B-cell lymphoma 2 inhibitor. The FDA granted the application Priority Review and assigned a PDUFA goal date of March 14, 2024.

Clinical &

Research

Abecma

Results from the preplanned final progression-free survival (PFS) analysis of the pivotal Phase 3, open-label, global, randomized controlled KarMMa-3 trial demonstrated a significantly improved PFS maintained with Abecma compared to standard regimens, with a 51% reduction in the risk of disease progression or death.

 

Breyanzi

First disclosure of primary analysis results from the high-risk, second-line cohort of the Phase 2 TRANSCEND FL trial evaluating Breyanzi in patients with relapsed or refractory FL demonstrated 95.7% complete response for patients with high-risk relapsed or refractory FL treated in a second-line setting.

 

Reblozyl

Updated results from the primary analysis of the Phase 3 COMMANDS trial, comparing Reblozyl versus epoetin alfa for the treatment of anemia in erythropoiesis stimulating agent (ESA)-naïve patients with lower-risk myelodysplastic syndromes who may require red blood cell transfusions, confirmed positive outcome of the interim analysis with superior efficacy and durability compared to ESAs.

FULL YEAR FINANCIAL RESULTS

All comparisons are made versus the same period in 2022 unless otherwise stated.

  • Bristol Myers Squibb posted revenues of $45.0 billion, a decrease of 2%, both on a reported and when adjusted for foreign exchange basis, primarily due to lower sales of Revlimid, partially offset by higher sales of our new product portfolio and Opdivo.
  • U.S. revenues decreased 1% to $31.6 billion due to lower sales of Revlimid resulting from generic erosion and, as previously disclosed, an increase in the number of patients receiving free drug product for Revlimid, and to a lesser extent Pomalyst, from the Bristol Myers Squibb Patient Assistance Foundation, a separate and independent 501(c)(3) entity to which BMS donates products. This was partially offset by an increase in demand for Opdivo, Eliquis and new product portfolio.
  • International revenues decreased 6% to $13.5 billion, or 5% when adjusted for foreign exchange impacts, primarily due to lower sales of Revlimid and Eliquis, partially offset by an increase in demand for Opdivo and new product portfolio.
  • On a GAAP basis, gross margin decreased from 78.0% to 76.2% and on a non-GAAP basis, gross margin decreased from 78.8% to 76.6%, primarily due to product mix and lower hedge settlement gains.
  • On a GAAP and non-GAAP basis, marketing, selling and administrative expenses decreased 1% to $7.8 billion and $7.7 billion, respectively.
  • On a GAAP basis, research and development expenses decreased 2% to $9.3 billion. On a non-GAAP basis, research and development expenses decreased 1% to $9.1 billion.
  • On a GAAP and non-GAAP basis, Acquired IPRD increased 12% to $913 million. On a GAAP and non-GAAP basis, licensing income was $142 million during the year compared to $103 million in 2022.
  • On a GAAP basis, amortization of acquired intangible assets decreased 6% to $9.0 billion. The decrease was primarily due to the Abraxane marketed product right being fully amortized in the fourth quarter of 2022.
  • On a GAAP basis, effective tax rate changed from 17.7% to 4.7% primarily due to the receipt of a non-U.S. tax ruling regarding the deductibility of a statutory impairment and changes in income tax reserves, valuation allowances and IRS guidance regarding deductibility of certain non-U.S. research and development expenses. On a non-GAAP basis, the effective tax rate changed from 15.3% to 14.7%.
  • The company reported on a GAAP basis net earnings attributable to Bristol Myers Squibb of $8.0 billion, or $3.86 per share, compared to $6.3 billion, or $2.95 per share. In addition to the items above, the GAAP EPS was impacted by lower losses on equity investments as well as litigation and other settlement income in 2023. On a non-GAAP basis, net earnings attributable to Bristol Myers Squibb were $15.6 billion, or $7.51 per share, compared to $16.5 billion, or $7.70 per share. In addition to the non-GAAP drivers noted above, the non-GAAP EPS was impacted by higher royalty and investment income, as well as lower weighted-average common shares outstanding.

FULL YEAR PRODUCT REVENUE HIGHLIGHTS

($ amounts in millions)

 

Year Ended December 31,

2023

 

% Change from Year

Ended December 31,

2022

 

% Change from

Year Ended

December 31,

2022 Ex-F/X**

 

 

U.S.(c)

 

Int’l

 

WW(d)

 

U.S.(c)

 

Int’l

 

WW(d)

 

Int’l

 

WW(d)

In-Line Products

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Eliquis

 

$

8,592

 

$

3,614

 

$

12,206

 

10%

 

(10)%

 

4%

 

(10)%

 

3%

Opdivo

 

 

5,283

 

 

3,726

 

 

9,009

 

10%

 

8%

 

9%

 

11%

 

10%

Orencia

 

 

2,754

 

 

847

 

 

3,601

 

4%

 

3%

 

4%

 

6%

 

5%

Pomalyst/Imnovid

 

 

2,357

 

 

1,084

 

 

3,441

 

(3)%

 

2%

 

(2)%

 

3%

 

(1)%

Yervoy

 

 

1,388

 

 

850

 

 

2,238

 

6%

 

3%

 

5%

 

5%

 

6%

Sprycel

 

 

1,446

 

 

484

 

 

1,930

 

(3)%

 

(28)%

 

(11)%

 

(25)%

 

(10)%

Mature and other products (a)

 

 

772

 

 

1,123

 

 

1,895

 

3%

 

(13)%

 

(7)%

 

(11)%

 

(6)%

Total In-Line Products

 

 

22,592

 

 

11,728

 

 

34,320

 

6%

 

(3)%

 

3%

 

(2)%

 

4%

New Product Portfolio

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Reblozyl

 

 

811

 

 

197

 

 

1,008

 

37%

 

56%

 

41%

 

54%

 

40%

Opdualag

 

 

617

 

 

10

 

 

627

 

*

 

N/A

 

*

 

N/A

 

*

Abecma

 

 

358

 

 

114

 

 

472

 

21%

 

25%

 

22%

 

24%

 

21%

Zeposia

 

 

324

 

 

110

 

 

434

 

83%

 

51%

 

74%

 

47%

 

72%

Breyanzi

 

 

303

 

 

61

 

 

364

 

*

 

97%

 

100%

 

*

 

*

Camzyos

 

 

226

 

 

5

 

 

231

 

*

 

N/A

 

*

 

N/A

 

*

Sotyktu

 

 

157

 

 

13

 

 

170

 

*

 

N/A

 

*

 

N/A

 

*

Onureg

 

 

117

 

 

51

 

 

168

 

23%

 

76%

 

35%

 

72%

 

35%

Inrebic

 

 

74

 

 

36

 

 

110

 

7%

 

*

 

29%

 

*

 

29%

Augtyro

 

 

1

 

 

 

 

1

 

N/A

 

N/A

 

N/A

 

N/A

 

N/A

Total New Product Portfolio

 

 

2,988

 

 

597

 

 

3,585

 

80%

 

63%

 

77%

 

61%

 

76%

Total In-Line and New Product Portfolio

 

 

25,580

 

 

12,325

 

 

37,905

 

12%

 

(1)%

 

7%

 

—%

 

8%

Recent LOE Products (b)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Revlimid

 

 

5,266

 

 

831

 

 

6,097

 

(37)%

 

(49)%

 

(39)%

 

(47)%

 

(39)%

Abraxane

 

 

709

 

 

295

 

 

1,004

 

22%

 

28%

 

24%

 

39%

 

27%

Total Recent LOE Products

 

 

5,975

 

 

1,126

 

 

7,101

 

(33)%

 

(39)%

 

(34)%

 

(36)%

 

(34)%

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Total Revenues

 

$

31,555

 

$

13,451

 

$

45,006

 

(1)%

 

(6)%

 

(2)%

 

(5)%

 

(2)%

Contacts

For more information, contact:
Media: media@bms.com
Investor Relations: investor.relations@bms.com

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