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Aptose Biosciences (TSE:APS)
TSX:APS
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Aptose Biosciences (APS) Drug Pipeline

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Drug Name
Condition
Stage
Status
Study Name
Trial Start Date
Article
Cg-806
Acute Myeloid Leukemia, Myelodysplastic Syndromes
Phase I
Terminated
A Study of CG-806 in Patients With Relapsed or Refractory AML or Higher-Risk MDS
Jul 13, 2020
Cg-806
Chronic Lymphocytic Leukemia, Small Lymphocytic Lymphoma, Non-Hodgkin's Lymphoma
Phase I
Terminated
A Study of CG-806 in Patients With Relapsed or Refractory CLL/SLL or Non-Hodgkin's Lymphomas
Mar 25, 2019
Tuspetinib, Venetoclax Oral Tablet, Azacitidine For Intravenous Infusion
Leukemia, Myeloid, Acute, Relapsed Adult Aml, Refractory Aml, Chronic Myelomonocytic Leukemia, Myelodysplastic Syndrome With Excess Blasts-2
Phase I/II
Recruiting
Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Tuspetinib (HM43239) in Patients With Relapsed or Refractory Acute Myeloid Leukemia
Jan 28, 2019

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
    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 Aptose Biosciences (APS) have in its pipeline
      APS is currently developing the following drugs: Cg-806, Cg-806, Tuspetinib, Venetoclax Oral Tablet, Azacitidine For Intravenous Infusion. These drug candidates are in various stages of clinical development as the company works toward FDA approval.
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