ALTH Related FDA
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FTC Clears Spectrum's (SPPI) Acquisition of Allos (ALTH) Acquisition
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Allos (ALTH) Says CHMP Reaffirms Negative Opinion on FOLOTYN MAA
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Allos Therapeutics (ALTH) Submits Request for Re-Examination of FOLOTYN Negative Opinion by CHMP
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Allos Therapeutics (ALTH) Says EMA CHMP Recommends Against Approval for FOLOTYN as PTCL Treatment
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Allos Therapeutics (ALTH) Updates on FOLOTYN PROPEL
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Allos (ALTH) Reports Publication of Encouraging FOLOTYN Data
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Allos (ALTH) Updates on COMPLETE for Futher PTCL Treatment Understanding
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Allos Therapeutics (ALTH) Presents FOLOTYN Data at EHA Congress
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Ariad (ARIA) May Have Been Best at ASH Meeting
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Allos Therapeutics (ALTH) Presents Strong Data from PROPEL of FOLOTYN in Patients with Relapsed PTCL
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Allos Therapeutics (ALTH) Announces Encouraging Data from FOLOTYN PROPEL in Patients with PTCL
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Allos Therapeutics (ALTH) To Present Data for FOLOTYN Phase 2b in Patients with Stage IIIB/IV NSCLC
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Allos Therapeutics (ALTH) To Present Five Abstracts of FOLOTYN Data on Blood Cancers at 52nd ASH Annual Meeting
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Allos Therapeutics (ALTH) Announces the EC Grants Orphan Designation to HL Treatment Pralatrexate
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Allos Therapeutics (ALTH) Announces Strong Results in FOLOTYN Phase 2b
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Allos Therapeutics (ALTH) Gets Orphan Designation from EC for CTCL Treatment Pralatrexate
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Allos Therapeutics (ALTH) Presents Data from FOLOTYN Phase 1
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Allos Therapeutics (ALTH) Announces Strong Data Related to PROPEL Trial of FOLOTYN In Patients with PTCL
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Allos Therapeutics (ALTH) Gets Orphan Drug Designation from U.S. FDA for Pralatrexate
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Allos Thera (ALTH) Updates on Pivotal PROPEL Trail of FOLOTYN
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Shares of Allos Therapeutics (ALTH) Give Back After Strong Opening
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Allos Therapeutics' (ALTH) FOLOTYN First and Only FDA-Approved Therapy for Relapsed or Refractory Peripheral T-cell Lymphoma
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Allos Therapeutics (ALTH) October volatility elevated into FDA meeting
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Allos Therapeutics (ALTH) Higher Following FDA Panel Recommendation of FOLOTYN
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FDA Panel Backs Allos Therapeutics (ALTH) lymphoma drug Folotyn
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Allos Therapeutics (ALTH) Announces FDA Advisory Committee to Review Pralatrexate for the Treatment of Patients with Relapsed or Refractory Peripheral T-cell Lymphoma
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Allos Therapeutics (ALTH) Updates Phase 2 PROPEL Study At ASCO
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Allos Therapeutics (ALTH) Announces FDA Accepts Pralatrexate NDA for Filing and Grants the Application Priority Review Status
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Allos Therapeutics' (ALTH) Pralatrexate Granted Orphan Medicinal Product Designation for the Treatment of Bladder Cancer
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Allos Therapeutics (ALTH) Announces Positive Phase 2 PROPEL Trial of Pralatrexate
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Allos Therapeutics (ALTH) Reports Preliminary Top Line Results from PROPEL
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Allos Therapeutics (ALTH) Granted FDA Orphan Drug Designation for Treatment of Patients with Follicular Lymphoma
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Allos Therapeutics (ALTH) Announces FDA Grants Orphan Drug Status for Pralatrexate
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Allos Therapeutics (ALTH) Completes Patient Enrollment in Pivotal Phase 2 PROPEL Trial of PDX in Patients with Peripheral T-cell Lymphoma
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Allos Therapeutics (ALTH) Said Efaproxyn Failed to Meet Primary Endpoint
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Allos Therapeutics (ALTH) Initiates Phase I/II Study of PDX and Gemcitabine
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Allos Therapeutics (ALTH) Announces Presentation of Phase 1/2 Trials of PDX in Patients with Relapsed or Refractory non-Hodgkin's Lymphoma and Hodgkin's Disease
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Needham Highlights Biotech Companies Presenting at the Upcoming American Society of Hematology
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Allos Therapeutics (ALTH) Says Phase 1/2 Results of PDX to be Presented at American Society of Hematology Annual Meeting
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Allos Therapeutics (ALTH) Receives FDA Fast Track Designation for PDX
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Needham Analyst Discusses Partnering Opportunities in Biotech
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Allos Therapeutics (ALTH) Announces Positive Pre-Clinical Study of EFAPROXYN
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Allos Therapeutics (ALTH) Interim Analysis Supports Continuation of Phase 3 Trial
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Needham issues a note focusing on biotech stocks with upcoming milestones in March
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ALTH Said Pralatrexate Plus Gemcitabine Proves Superior to Methotrexate Plus Cytarabine
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ALTH Said EFAPROXYN Extends Survival n Patients With Brain Metastases
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ALTH Said EFAPROXYN May Improve Survival in Lung Cancer Patients
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