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Telitacicept
Primary Sjogren's Disease
Phase III
Recruiting
Phase 3 Study of Telitacicept in Active Primary Sjögren's Disease
Feb 04, 2026
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Telitacicept
Systemic Lupus Erythematosus
Phase III
Withdrawn
A Study of Telitacicept for the Treatment of Moderately to Severely Active Systemic Lupus Erythematosus (REMESLE-2)
Jun 07, 2024
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Vcar33
Leukemia, Myeloid, Acute
Phase I/II
Terminated
Donor-Derived Anti-CD33 CAR T Cell Therapy (VCAR33) in Patients With Relapsed or Refractory AML After Allogeneic Hematopoietic Cell Transplant
Jul 19, 2023
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Telitacicept
Systemic Lupus Erythematosus
Phase III
Terminated
A Study of Telitacicept for the Treatment of Moderately to Severely Active Systemic Lupus Erythematosus (REMESLE-1)
Mar 23, 2022
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Vor33, Mylotarg
Leukemia, Myeloid, Acute, Myelodysplastic Syndromes
Phase I/II
Terminated
Allogeneic Engineered Hematopoietic Stem Cell Transplant (HCT) Lacking the CD33 Protein, and Post-HCT Treatment With Mylotarg, for Patients With CD33+ AML or MDS
Mar 25, 2021
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FAQ
What are the FDA phases for drug approval?
The FDA approval process for new drugs is divided into several phases:
a. Preclinical testing
b. Phase 1 – Safety and dosage
c. Phase 2 – Effectiveness and side effects
d. Phase 3 – Confirmation of effectiveness, monitoring of adverse reactions, and comparison with existing treatments
e. Phase 4 – Post-marketing studies to track long-term safety and effectiveness
a. Preclinical testing
b. Phase 1 – Safety and dosage
c. Phase 2 – Effectiveness and side effects
d. Phase 3 – Confirmation of effectiveness, monitoring of adverse reactions, and comparison with existing treatments
e. Phase 4 – Post-marketing studies to track long-term safety and effectiveness
What is a clinical trial?
A clinical trial is a carefully designed study in which researchers test a drug, treatment, or medical device in people to evaluate its safety, effectiveness, and potential side effects. These trials are essential for determining whether a new treatment should be approved for widespread use.
What drugs does Vor Biopharma (VOR) have in its pipeline
VOR is currently developing the following drugs: Telitacicept, Telitacicept, Telitacicept. These drug candidates are in various stages of clinical development as the company works toward FDA approval.