Citius Pharmaceuticals, Inc. Submits Biologics License Application to the U.S. Food and Drug Administration for Denileukin Diftitox for the Treatment of Patients with Persistent or Recurrent Cutaneous T-Cell Lymphoma

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More Recent News About Citius Pharmaceuticals Inc.

Citius Pharmaceuticals Announces Closing of $15 Million Registered Direct Offering
Citius Pharmaceuticals Announces $15 Million Registered Direct Offering
Citius Pharmaceuticals Announces Addition of City of Hope to UMN's Phase 1 Trial of LYMPHIR in Combination with CAR-T for the Treatment of B-Cell Lymphoma
Citius Pharmaceuticals to Present at the LD Micro Invitational XIV Investor Conference
Citius Pharmaceuticals Announces FDA Acceptance of the BLA Resubmission of LYMPHIR(TM) (Denileukin Diftitox) for the Treatment of Adults with Relapsed or Refractory Cutaneous T-Cell Lymphoma
Citius Pharmaceuticals, Inc. Secures $2.4 million through New Jersey Economic Development Program
Citius Pharmaceuticals Announces Filing of Form S-3 Shelf Registration Statement to Replace Expiring Prior Shelf Registration
Citius Pharmaceuticals to Participate in Upcoming BIO CEO and Sidoti Investor Conferences

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