Other Clinical Trial - A Study of Rebastinib (DCC-2036) in Combination

See also
Status	Clinical Trial	Phase
Completed	`NCT03601897` - A Phase 1b/2 Study of Rebastinib (DCC-2036) in Combination With Paclitaxel in Patients With Advanced or Metastatic Solid Tumors	Phase 1/Phase 2
Recruiting	`NCT05194982` - A Study of BL-B01D1 in Patients With Locally Advanced or Metastatic Solid Tumor	Phase 1
Recruiting	`NCT05461768` - A Study of BL-M07D1 in Patients With Locally Advanced or Metastatic HER2 Positive/Low Expression Breast Cancer and Other Solid Tumors	Phase 1

See also

Status

Clinical Trial

Phase

Completed

NCT03601897 - A Phase 1b/2 Study of Rebastinib (DCC-2036) in Combination With Paclitaxel in Patients With Advanced or Metastatic Solid Tumors

Phase 1/Phase 2

Recruiting

NCT05194982 - A Study of BL-B01D1 in Patients With Locally Advanced or Metastatic Solid Tumor

Phase 1

Recruiting

NCT05461768 - A Study of BL-M07D1 in Patients With Locally Advanced or Metastatic HER2 Positive/Low Expression Breast Cancer and Other Solid Tumors

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	NCT03717415
Study type	Interventional
Source	Deciphera Pharmaceuticals LLC
Contact
Status	Completed
Phase	Phase 1/Phase 2
Start date	January 2, 2019
Completion date	November 1, 2022

A Study of Rebastinib (DCC-2036) in Combination With Carboplatin in Patients With Advanced or Metastatic Solid Tumors

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms