OTC$LIANY

Lianbio-Adr · Q2 2023 earnings

Q2 2023 earnings · · Investor relations

Briefing

LianBio's financial performance in Q2 2023 reflected a decrease in research and development expenses, offset by increased general and administrative costs, resulting in a reduced net loss compared to the same period last year.

LianBio reported a net loss of $21.6 million for the second quarter of 2023, compared to a net loss of $42.4 million for the second quarter of 2022. Research and development expenses decreased to $9.5 million from $28.6 million year-over-year, while general and administrative expenses increased slightly to $15.6 million from $14.6 million year-over-year. The company's cash, cash equivalents, and marketable securities totaled $267.3 million, providing a cash runway into the first half of 2025.

  • Mavacamten NDA under priority review with China NMPA.
  • Phase 3 EXPLORER-CN trial of mavacamten in Chinese patients with oHCM met the primary endpoint.
  • Data from EXPLORER-CN trial to be presented at the European Society of Cardiology Congress 2023.
  • Cash, cash equivalents, and marketable securities totaled $267.3 million, providing a runway into the first half of 2025.

Headline financials

Total Revenue

$0.00

No prior period
EPS (adj)

-$0.21

Previous: -$0.39+46.2%
Capital Expenditures

-$49.6K

Previous: $329K-115.1%
Free Cash Flow

-$19.2M

Previous: -$39.7M+51.7%
Net Income

-$21.6M

Previous: -$42.4M+49.0%
Operating Income

-$25M

Previous: -$43.1M+41.9%
Gross Profit

-$297K

No prior period
Cash & Equivalents

$104M

Previous: $134M-22.5%
Total Assets

$279M

Previous: $372M-25.0%
R&D Expense

$9.35M

No prior period
Stock-Based Comp

$4.49M

Previous: $4.53M-0.8%

Revenue & EPS history

Lianbio-Adr · Revenue · Quarterly

$0

Q2 2023
Beat estimate in 0 of 1 quarters(0%)
ActualEstimate

Forward guidance

LianBio anticipates several key milestones, including the potential NDA approval and commercial launch of mavacamten in China, topline data from the Phase 3 LIBRA trial of TP-03, and initiation of a pivotal Phase 2 trial of infigratinib. These steps are expected to drive growth and expand treatment options of cardiovascular, oncology, ophthalmology, and inflammatory disease indications.

Tailwinds

  • Initiating Phase 3 ODYSSEY-HCM trial of mavacamten in non-obstructive HCM in China in mid-2024.
  • Anticipating NDA approval for mavacamten in China in mid-2024 and commercial launch in the second half of 2024.
  • Expecting to launch mavacamten in Singapore and Macau in the fourth quarter of 2023.
  • Planning to file NDAs to support mavacamten approval in Taiwan and Thailand in the fourth quarter of 2023.
  • Expecting to report topline data from the Phase 3 LIBRA trial of TP-03 in Chinese patients with Demodex blepharitis in the fourth quarter of 2023.

Headwinds

  • Clinical trials may not produce expected results.
  • Regulatory approvals are subject to uncertainty and delays.
  • Dependence on partners for data and regulatory submissions.
  • Competition from other biotechnology and pharmaceutical companies.
  • General market conditions and changing laws and regulations may impact results.

Historical earnings impact

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

Avg. return before/after earnings

Based on 12 quarterly earnings reports · overlaid with Q2 2023

Historical avgQ2 2023

+8.4%

Avg return

Earnings day

+8.4%

Avg return

5 days after

-3.1%

Avg return

30 days after

77%

10 / 13 earnings

Positive

+17.7%

Q4 2020

Best reaction

-4.1%

Q1 2023

Worst reaction

Earnings price reactions
QuarterReport dateReaction (Day 0)+5 days+30 days
Q4 2024-2.2%-6.7%-7.4%
Q3 2023+0.7%+1.5%+4.2%
Q2 2023+2.7%+0.0%-9.7%
Q1 2023-4.1%+4.6%+17.7%
Q4 2022-1.2%+17.4%+18.0%
Q3 2022+17.5%+38.9%+7.1%
Q2 2022+11.1%-1.5%-3.0%
Q1 2022+9.3%+29.8%+28.4%
Q4 2021+3.9%+26.1%+7.3%
Q2 2021+17.7%+0.4%-17.3%
Q3 2021+17.7%+0.4%-17.3%
Q4 2020+17.7%+0.4%-17.3%
Q1 2021+17.7%-2.4%-50.4%
Q3 2020

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