Rallybio Corporation (USD) Rallybio Corporation, a clinical-stage biotechnology company, engages in discovering, developing, manufacturing, and delivering therapies that enhance the lives of patients suffering from severe and rare diseases. Its lead product candidate is RLYB212, a monoclonal anti-HPA-1a antibody that is in Phase I clinical trial for the prevention of fetal and neonatal alloimmune thrombocytopenia (FNAIT). The company is also developing RLYB211, a polyclonal anti-HPA-1a antibody that is in a Phase 1/2 clinical trial for the prevention of FNAIT; RLYB114, a pegylated complement factor 5 (C5)-targeted Affibody molecule in preclinical development for the treatment of complement-mediated ophthalmic diseases; and RLYB116, a subcutaneously administered inhibitor of C5 for the treatment of patients with paroxysmal nocturnal hemoglobinuria and generalized myasthenia gravis. Rallybio has collaboration with Exscientia for the development of small molecule therapeutics for rare diseases. Rallybio Corporation was founded in 2018 and is headquartered in New Haven, Connecticut.

Rallybio Corporation (USD) Active

234 Church Street, New Haven, CT, US, 06510

Stock Price USD

Price Change

Last Dividend USD

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RLYB's stock peer is ANTX (AN2 Therapeutics, Inc.)

RLYB's stock peer is CCCC (C4 Therapeutics, Inc.)

RLYB's stock peer is CGEM (Cullinan Oncology, Inc.)

RLYB's stock peer is ELYM (Eliem Therapeutics, Inc.)

RLYB's stock peer is EWTX (Edgewise Therapeutics, Inc.)

RLYB's stock peer is GLUE (Monte Rosa Therapeutics, Inc.)

RLYB's stock peer is IPSC (Century Therapeutics, Inc.)

RLYB's stock peer is MLYS (Mineralys Therapeutics, Inc.)

RLYB's stock peer is MNOV (MediciNova, Inc.)

RLYB's stock peer is MOLN (Molecular Partners AG)

RLYB's stock peer is OPT (Opthea Limited)

RLYB's stock peer is PHVS (Pharvaris N.V.)

RLYB's stock peer is PMVP (PMV Pharmaceuticals, Inc.)

RLYB's stock peer is THRD (Third Harmonic Bio, Inc.)

Healthcare Biotechnology

Rallybio Corporation, a clinical-stage biotechnology company, engages in discovering, developing, manufacturing, and delivering therapies that enhance the lives of patients suffering from severe and rare diseases. Its lead product candidate is RLYB212, a monoclonal anti-HPA-1a antibody that is in Phase I clinical trial for the prevention of fetal and neonatal alloimmune thrombocytopenia (FNAIT). The company is also developing RLYB211, a polyclonal anti-HPA-1a antibody that is in a Phase 1/2 clinical trial for the prevention of FNAIT; RLYB114, a pegylated complement factor 5 (C5)-targeted Affibody molecule in preclinical development for the treatment of complement-mediated ophthalmic diseases; and RLYB116, a subcutaneously administered inhibitor of C5 for the treatment of patients with paroxysmal nocturnal hemoglobinuria and generalized myasthenia gravis. Rallybio has collaboration with Exscientia for the development of small molecule therapeutics for rare diseases. Rallybio Corporation was founded in 2018 and is headquartered in New Haven, Connecticut.

100%

Dcf Rating

20%

Return On Equity

20%

Return On Assets

80%

Debt To Equity

20%

Price To Earnings

80%

Price To Book

Dividend Stats Yield is calculated via trailing-12-month period

Ex-Dividend	Payment Date	Dividend	Yield	Dividend Frequency
Dividend Data Not Exist

Recent News

Rallybio Reports First Quarter 2025 Financial Results and Provides Business Updates

NEW HAVEN, Conn.--(BUSINESS WIRE)--Rallybio Corporation (Nasdaq: RLYB), a clinical-stage biotechnology company translating scientific advances into transformative therapies for patients with devastating rare diseases, today reported first quarter financial results for the period ended March 31, 2025, and provided an update on recent company developments. “We are focused on advancing RLYB116 into a confirmatory pharmacokinetic/pharmacodynamic study this quarter, and believe that data from this s.

2025-05-08 08:00:00

Rallybio to Discontinue Development of RLYB212 for Prevention of FNAIT

NEW HAVEN, Conn.--(BUSINESS WIRE)--Rallybio Corporation (Nasdaq: RLYB), a clinical-stage biotechnology company translating scientific advances into transformative therapies for patients with devastating rare diseases, today announced the discontinuation of the RLYB212 program for the prevention of fetal and neonatal alloimmune thrombocytopenia (FNAIT). The Company's decision to discontinue RLYB212 development was based on pharmacokinetic (PK) data from the Phase 2 clinical trial demonstrating t.

2025-04-08 08:00:00

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