OncoSec Provides Encouraging Interim Data from Ongoing KEYNOTE-890 Study of TAVO in Combination with KEYTRUDA® for the Treatment of Heavily Pretreated Chemotherapy/Radiotherapy Refractory Metastatic Triple Negative Breast Cancer

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More Recent News About OncoSec Medical Incorporated

OncoSec Announces Closing of $1.33 Million Registered Direct Offering Priced At-The-Market Under Nasdaq Rules
OncoSec Announces $1.33 Million Registered Direct Offering Priced At-The-Market Under Nasdaq Rules
OncoSec is encouraged after FDA meeting to discuss proposed neoadjuvant melanoma clinical program
OncoSec Receives $3.49 Million to Strengthen its Balance Sheet After Selling its Net Operating Loss Tax Benefits Through The New Jersey Economic Development Authority NOL Program
OncoSec Announces Closing of $2 Million Registered Direct Offering Priced At-The-Market Under Nasdaq Rules
OncoSec Announces $2 Million Registered Direct Offering Priced At-The-Market Under Nasdaq Rules
OncoSec Announces Clinical Data of the KEYNOTE-695 Trial Assessing TAVO(TM)-EP in Combination with KEYTRUDA® (pembrolizumab) in Patients with Advanced Melanoma Refractory to anti-PD-1 Treatment
OncoSec to Present at the RHK Capital Disruptive Growth Conference on December 6, 2022

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