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NASDAQ:AVBP

ArriVent BioPharma Q4 2024 Earnings Results & Report

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$16.09 -0.37 (-2.25%)
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ArriVent BioPharma beat analyst earnings expectations in its Q4 2024 results, released March 3, 2025. The company reported EPS of -$0.60 versus the -$0.78 consensus estimate.

Earnings Announcement Details

Quarter
Q4 2024
Report Date
Time
Before Market Opens
Conference Call
7:00 AM ET

ArriVent BioPharma EPS Results

Actual EPS
-$0.60
Consensus EPS
-$0.78
Beat/Miss
Beat by +$0.18
One Year Ago EPS
N/A
EPS Beat Rate
2 of last 8 quarters

ArriVent BioPharma Revenue Results

Actual Revenue
N/A
Expected Revenue
N/A
Beat/Miss
N/A
YoY Revenue Growth
N/A

Upcoming Earnings

ArriVent BioPharma's Q3 2026 earnings is estimated for Monday, November 16, 2026, based on past reporting schedules, with a conference call scheduled on Thursday, November 12, 2026 at 4:00 PM ET. Check back for transcripts, audio, and key financial metrics as they become available.

ArriVent BioPharma Q4 2024 Earnings FAQ

ArriVent BioPharma (NASDAQ:AVBP) reported earnings of -$0.60 per share for Q4 2024, beating the consensus estimate of -$0.78. The report was announced on Monday, March 3, 2025.

ArriVent BioPharma's next earnings date is estimated for Monday, November 16, 2026. MarketBeat tracks confirmed and estimated earnings dates for ArriVent BioPharma on the company's earnings history page.

ArriVent BioPharma Earnings Headlines

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About ArriVent BioPharma

ArriVent BioPharma (NASDAQ:AVBP) is a clinical-stage biopharmaceutical company focused on developing and commercializing precision medicines for patients with genetically defined cancers. The company seeks to identify promising therapies developed in other regions and advance them through clinical development and regulatory approval in the United States and other markets.

ArriVent’s lead product candidate is furmonertinib, an oral, irreversible epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor designed to target specific EGFR mutations in non-small cell lung cancer, including EGFR exon 20 insertion mutations. Furmonertinib has been approved in China for certain EGFR-mutated non-small cell lung cancer indications and is being evaluated by ArriVent in additional patient populations and geographies.

The company obtained rights to develop and commercialize furmonertinib outside Greater China through a partnership with Allist Pharmaceuticals. ArriVent is headquartered in the United States and is advancing its programs through clinical trials intended to support potential regulatory submissions in the United States and other international markets. Its pipeline and development strategy are centered on targeted oncology therapies for patients whose tumors have actionable genetic alterations.

View ArriVent BioPharma Profile