NASDAQ$ONC

BeiGene Ltd-ADR · Q2 2021 earnings

Q2 2021 earnings · · Investor relations

Briefing

BeiGene reported a strong second quarter in 2021, marked by significant revenue growth and progress in clinical development.

BeiGene reported a notable increase in product revenue, reaching $138.6 million in the second quarter of 2021, a 111% increase compared to the same period last year. The company saw growth in sales of BRUKINSA and tislelizumab, and continued advancements in its pipeline, including positive Phase 3 trial data and new regulatory approvals.

  • Product revenue increased by 111% year-over-year, reaching $138.6 million.
  • Positive interim Phase 3 BRUKINSA data reported from SEQUOIA and ALPINE trials.
  • Two Phase 3 clinical trials initiated for ociperlimab in NSCLC.
  • Plans announced to expand global manufacturing capabilities with a U.S. facility.

Headline financials

Total Revenue

$150M

Previous: $65.6M+128.5%
EPS (adj)

-$5.23

Previous: -$4.31-21.3%
R&D Expenses

$356M

Previous: $286M+24.5%
SG&A Expenses

$232M

Previous: $124M+87.3%
Capital Expenditures

-$80.9M

Previous: -$54.1M-49.5%
Free Cash Flow

-$376M

Previous: -$659M+42.9%
Net Income

-$480M

Previous: -$335M-43.3%
Operating Income

-$475M

Previous: -$359M-32.3%
Gross Profit

$114M

Previous: $51.3M+121.6%
Cash & Equivalents

$1.78B

Previous: $1.35B+32.1%
Total Assets

$5.52B

Previous: $3.9B+41.5%
Stock-Based Comp

$64.8M

Previous: $45.5M+42.5%

Revenue & EPS history

BeiGene · Revenue · Quarterly

$150M

Q2 2021+128.5%vs Q2 2020
Beat estimate in 6 of 14 quarters(43%)
ActualEstimate

Revenue by segment

BeiGene · $42.4M total across 1 segment · Q2 2021

  • BRUKINSA
    $42.4M+508.3%

Forward guidance

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 and other federal securities laws, including statements regarding clinical data for BeiGene’s drug candidates and approvals of its medicines; the conduct of late-stage clinical trials and expected data readouts; additional planned product approvals and launches; the advancement of and anticipated clinical development, regulatory milestones and commercialization of BeiGene’s medicines and drug candidates; the success of BeiGene’s commercialization efforts and revenue growth; the expected capacities and completion dates for the Company’s manufacturing facilities under construction; the timeline for the Company to complete its proposed public offering and listing on the STAR Market of the Shanghai Stock Exchange, if at all; the impact of the COVID-19 pandemic on the Company’s clinical development, regulatory, commercial and other operations; BeiGene’s plans and the expected events and milestones under the caption “Recent Business Highlights and Upcoming Milestones”; and BeiGene’s plans, commitments, aspirations and goals under the captions “About BeiGene”.

Tailwinds

  • Continued clinical evidence for the best-in-class potential of BRUKINSA.
  • Expanded list of indications for tislelizumab in China.
  • Progress with our differentiated Phase 3 stage, anti-TIGIT antibody, ociperlimab.
  • Expansion of global manufacturing capabilities through establishment of a U.S. facility
  • Listing of the Company’s ordinary shares on the STAR Market is expected to be completed in 2021, subject to market conditions and additional regulatory approvals

Headwinds

  • The Company expects that the worldwide health crisis of COVID-19 will continue to have a negative impact on its operations, including commercial sales, regulatory interactions, inspections, filings, and clinical trial recruitment, participation, and data read outs.
  • BeiGene's ability to demonstrate the efficacy and safety of its drug candidates
  • The clinical results for its drug candidates, which may not support further development or marketing approval
  • Actions of regulatory agencies, which may affect the initiation, timing and progress of clinical trials and marketing approval
  • BeiGene's ability to achieve commercial success for its marketed medicines and drug candidates, if approved

Historical earnings impact

How earnings announcements have historically affected this stock's price.

Avg. return before/after earnings

Based on 20 quarterly earnings reports · overlaid with Q2 2021

Historical avgQ2 2021

-0.1%

Avg return

Earnings day

+0.1%

Avg return

5 days after

-2.0%

Avg return

30 days after

40%

16 / 40 earnings

Positive

+15.9%

Q4 2023

Best reaction

-9.6%

Q1 2022

Worst reaction

Earnings price reactions
QuarterReport dateReaction (Day 0)+5 days+30 days
Q1 2026+5.3%+4.3%-9.4%
Q4 2025-8.5%-15.7%-19.6%
Q3 2025+3.4%+6.9%+0.5%
Q1 2025-3.9%-3.5%+5.8%
Q4 2024+7.5%-0.7%+3.2%
Q3 2024+1.4%-4.5%+1.4%
Q2 2024+6.8%+10.9%+11.7%
Q1 2024-2.0%-2.2%-4.9%
Q4 2023+15.9%+6.4%-0.0%
Q3 2023-0.5%+0.7%-12.6%
Q2 2023-0.3%-9.2%+1.2%
Q1 2023-5.7%-7.3%-14.2%
Q4 2022+4.2%+11.9%+2.9%
Q3 2022-0.2%+7.3%+4.2%
Q2 2022+14.6%+16.4%-1.7%
Q1 2022-9.6%-11.9%-12.9%
Q4 2021-2.5%-0.8%-10.8%
Q3 2021-2.3%-1.1%-15.9%
Q2 2021-6.3%-8.1%-2.0%
Q1 2021+2.2%+5.4%+15.7%
Q4 2020-4.4%-8.5%-3.0%
Q3 2020-3.6%-7.2%-26.8%
Q2 2020-2.9%-7.7%+5.8%
Q1 2020+1.0%+6.0%+9.6%
Q4 2019-2.3%-3.2%-21.8%
Q3 2019+2.9%+3.4%-6.5%
Q2 2019+1.6%+3.9%-7.8%
Q1 2019+14.2%+13.6%+4.3%
Q4 2018-2.1%+8.4%-5.7%
Q3 2018+1.4%-11.2%+10.4%
Q2 2018-3.7%-4.4%-4.7%
Q1 2018-5.2%+4.3%+20.9%
Q4 2017-4.8%+0.3%+11.3%
Q3 2017-5.5%-0.0%+10.4%
Q2 2017-7.3%-9.0%-7.4%
Q1 2017-1.3%+0.7%+3.9%
Q4 2016-2.8%-4.1%-3.1%
Q3 2016-4.7%+7.4%-19.5%
Q2 2016+0.8%+6.0%+11.0%
Q4 2015+5.9%
Q3 2015
Q2 2015
Q1 2015
Q4 2014
Q3 2014
Q2 2014
Q1 2014

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