Other Clinical Trial - Tolerability Study of Trichostatin A In Subjects

See also
	Status	Clinical Trial	Phase
	Recruiting	`NCT04926285` - Safety and Efficacy of Venetoclax With Escalating Doses of Omacetaxine in Patients With Acute Myeloid Leukemia Safety and Efficacy of Venetoclax With Escalating Doses of Omacetaxine in Patients With Acute Myeloid Leukemia (AML)	Phase 1
	Recruiting	`NCT06252298` - A Clinical Study of SCTC21C in Participants With CD38+ Hematologic Malignancies	Phase 1

See also

Status

Clinical Trial

Phase

Recruiting

NCT04926285 - Safety and Efficacy of Venetoclax With Escalating Doses of Omacetaxine in Patients With Acute Myeloid Leukemia Safety and Efficacy of Venetoclax With Escalating Doses of Omacetaxine in Patients With Acute Myeloid Leukemia (AML)

Phase 1

Recruiting

NCT06252298 - A Clinical Study of SCTC21C in Participants With CD38+ Hematologic Malignancies

Phase 1

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT03838926
Study type	Interventional
Source	Vanda Pharmaceuticals
Contact	Vanda Pharmaceuticals
Phone	202-734-3400
Email	clinicaltrials@vandapharma.com
Status	Recruiting
Phase	Phase 1
Start date	September 27, 2018
Completion date	September 2020

Tolerability Study of Trichostatin A In Subjects With Relapsed or Refractory Hematologic Malignancies

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms