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
Revenue & EPS history
Lianbio-Adr · Revenue · Quarterly
$0
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
+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
| Quarter | Report date | Reaction (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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