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Merus NV (MRUS) News & Sentiment

Merus N.V. (MRUS) Reports Q4 Loss, Lags Revenue Estimates
Merus N.V. (MRUS) Reports Q4 Loss, Lags Revenue Estimates
Merus N.V. (MRUS) Reports Q4 Loss, Lags Revenue Estimates
MRUS
zacks.comFebruary 27, 2025

Merus N.V. (MRUS) came out with a quarterly loss of $0.41 per share versus the Zacks Consensus Estimate of a loss of $0.95. This compares to loss of $1.09 per share a year ago.

Merus Announces Financial Results for the Fourth Quarter and Full Year 2024 and Provides Business Update
Merus Announces Financial Results for the Fourth Quarter and Full Year 2024 and Provides Business Update
Merus Announces Financial Results for the Fourth Quarter and Full Year 2024 and Provides Business Update
MRUS
globenewswire.comFebruary 27, 2025

-  Phase 3 registrational trials evaluating petosemtamab in combination with pembrolizumab in 1L PD-L1+ r/m HNSCC and petosemtamab monotherapy in 2/3L r/m HNSCC enrolling; expected to be substantially enrolled by YE25

Merus to Present at Upcoming Investor Conferences
Merus to Present at Upcoming Investor Conferences
Merus to Present at Upcoming Investor Conferences
MRUS
globenewswire.comFebruary 25, 2025

UTRECHT, The Netherlands and CAMBRIDGE, Mass., Feb. 25, 2025 (GLOBE NEWSWIRE) -- Merus N.V.

Merus to Present at Citi's 2025 Virtual Oncology Leadership Summit
Merus to Present at Citi's 2025 Virtual Oncology Leadership Summit
Merus to Present at Citi's 2025 Virtual Oncology Leadership Summit
MRUS
globenewswire.comFebruary 13, 2025

UTRECHT, The Netherlands and CAMBRIDGE, Mass., Feb. 13, 2025 (GLOBE NEWSWIRE) -- Merus N.V.

Time To Upgrade Merus N.V. To A 'Buy' After The Recent Selloff
Time To Upgrade Merus N.V. To A 'Buy' After The Recent Selloff
Time To Upgrade Merus N.V. To A 'Buy' After The Recent Selloff
MRUS
seekingalpha.comJanuary 20, 2025

Bizengri's recent approval gives MRUS the first approved therapy for NRG1+ cancers, which, I think, will be a valuable niche. Petosemtamab's recent Phase 2 data for HNSCC suggests it could also have blockbuster potential as long as its Phase 3 trials are successful as well. I also like MRUS's recent partnership with BHVN as it gives it optionality with new ADC programs that could have oncology applications.

Merus' Petosemtamab Monotherapy Interim Data Continues to Demonstrate Clinically Meaningful Activity in 2L+ r/m HNSCC
Merus' Petosemtamab Monotherapy Interim Data Continues to Demonstrate Clinically Meaningful Activity in 2L+ r/m HNSCC
Merus' Petosemtamab Monotherapy Interim Data Continues to Demonstrate Clinically Meaningful Activity in 2L+ r/m HNSCC
MRUS
globenewswire.comDecember 7, 2024

Petosemtamab in combination with pembrolizumab in 1L r/m PD-L1 expressing HNSCC ongoing with clinical data update planned for 2025

Merus Announces Publication of an Abstract on Petosemtamab as 2L+ treatment of r/m HNSCC at the ESMO Asia Congress 2024
Merus Announces Publication of an Abstract on Petosemtamab as 2L+ treatment of r/m HNSCC at the ESMO Asia Congress 2024
Merus Announces Publication of an Abstract on Petosemtamab as 2L+ treatment of r/m HNSCC at the ESMO Asia Congress 2024
MRUS
globenewswire.comDecember 1, 2024

– Petosemtamab 1500 mg monotherapy phase 2 interim data continues to demonstrate clinically meaningful activity in 2L+ HNSCC

Merus: Petosemtamab Set Up For December 2024 Data Presentation
Merus: Petosemtamab Set Up For December 2024 Data Presentation
Merus: Petosemtamab Set Up For December 2024 Data Presentation
MRUS
seekingalpha.comNovember 5, 2024

Merus is nearing a major milestone with zenocutuzumab's potential FDA approval for NRG1+ NSCLC/PDAC, with a PDUFA date of February 4, 2025. Petosemtamab, targeting 1st and 2nd-line HNSCC, shows promise with updated data to be presented at ESMO Asia Congress in December 2024. Financially stable with $782.9 million in cash, Merus has strategic partnerships with Gilead, Eli Lilly, Incyte, and Ono Pharmaceutical, funding operations into 2028.

Merus Receives FDA extension of PDUFA for zenocutuzumab
Merus Receives FDA extension of PDUFA for zenocutuzumab
Merus Receives FDA extension of PDUFA for zenocutuzumab
MRUS
globenewswire.comNovember 5, 2024

UTRECHT, The Netherlands and CAMBRIDGE, Mass., Nov. 05, 2024 (GLOBE NEWSWIRE) -- Merus N.V. (Nasdaq: MRUS) (Merus, the Company, we, or our), a clinical-stage oncology company developing innovative, full-length multispecific antibodies (Biclonics® and Triclonics®), today announced that the United States Food and Drug Administration (FDA) has extended the Prescription Drug User Fee Act (PDUFA) goal date for zenocutuzumab (Zeno) Biologics License Application (BLA) currently under priority review.

Merus N.V. (MRUS) Reports Q3 Loss, Tops Revenue Estimates
Merus N.V. (MRUS) Reports Q3 Loss, Tops Revenue Estimates
Merus N.V. (MRUS) Reports Q3 Loss, Tops Revenue Estimates
MRUS
zacks.comOctober 31, 2024

Merus N.V. (MRUS) came out with a quarterly loss of $0.95 per share versus the Zacks Consensus Estimate of a loss of $0.90. This compares to loss of $0.43 per share a year ago.