⭐️⭐️⭐️⭐️⭐️ "A total no brainer"

⭐️⭐️⭐️⭐️⭐️ "Love this, so easy."

Spots is the easy way to track your skin, mole and cancer changes.

Spots Global Cancer Trial Database for A Phase 1b Trial of ATRC-101 in Adults With Advanced Solid Malignancies

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: A Phase 1b Trial of ATRC-101 in Adults With Advanced Solid Malignancies

Official Title: A Phase 1b Dose Escalation and Expansion Trial to Investigate the Safety, Tolerability, Pharmacokinetics, and Biological Activity of ATRC-101 as Monotherapy and in Combination With Other Anticancer Agents in Adults With Advanced Solid Malignancies

Study ID: NCT04244552

Study Description

Brief Summary: ATRC-101-A01 is a Phase 1b, open-label dose escalation and expansion trial of ATRC-101, an engineered fully human immunoglobulin G, subclass 1 (IgG1) antibody derived from a naturally occurring human antibody. The safety, tolerability, PK, and biological activity of ATRC-101 will be characterized when administered every two weeks (Q2W) or every 3 weeks (Q3W) as a monotherapy or in combination with other anticancer agents.

Detailed Description: For the monotherapy cohorts, including the efficacy expansion cohorts, enrollment is restricted to adults with inoperable, locally advanced or metastatic breast cancer, NSCLC, CRC, ovarian cancer, and acral melanoma, which are all tumor types that have demonstrated ATRC-101 immunoreactivity on at least 50% of tested commercially procured archival specimens. For the pembrolizumab combination therapy cohort, enrollment is restricted to adults with inoperable, locally advanced or metastatic NSCLC, CRC (only MSI-H or dMMR), melanoma (with the exception of uveal melanoma), HCC, HNSCC, ESCC, UC or TNBC, that have been treated with anti-PD-1 or anti-PD-L1 therapy and have progressed radiographically or have achieved stable disease for a minimum of two months and who, in the judgment of their treating physicians, could benefit from a combination of ATRC 101 and pembrolizumab. For the PLD combination therapy cohort, enrollment is restricted to adult females with inoperable, locally advanced or metastatic high-grade serous epithelial ovarian, fallopian tube, or primary peritoneal cancer that is platinum resistant, defined as progression during or within 6 months of the last dose of platinum-based chemotherapy OR breast cancer that is refractory to other standard therapies. For target-enriched expansion cohorts, enrollment will be limited to participants with pretreatment tumor biopsies demonstrating ATRC-101 target expression above a predefined threshold by IHC at a central laboratory.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Mayo Clinic, Phoenix, Arizona, United States

The University of Arizona Cancer Center, Tucson, Arizona, United States

City of Hope, Duarte, California, United States

University of California, Los Angeles Hematology/Oncology, Los Angeles, California, United States

Georgetown University Medical Center, Washington, District of Columbia, United States

Mayo Clinic, Jacksonville, Florida, United States

Florida Cancer Specialists, Lake Mary, Florida, United States

University of Miami Hospital - Sylvester Comprehensive Cancer Center, Miami, Florida, United States

Massachusetts General Hospital, Boston, Massachusetts, United States

Mayo Clinic, Rochester, Minnesota, United States

Nebraska Cancer Specialists, Omaha, Nebraska, United States

Laura & Isaac Perlmutter Cancer Center at NYU Langone Health, New York, New York, United States

Icahn School of Medicine at Mount Sinai, New York, New York, United States

Oncology Specialists of Charlotte, Charlotte, North Carolina, United States

Carolina BioOncology, Huntersville, North Carolina, United States

Gabrail Cancer Center, Canton, Ohio, United States

Stephenson Cancer Center, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, United States

Vanderbilt University Medical Center, Nashville, Tennessee, United States

Oncology Consultants, PLLC, Houston, Texas, United States

Contact Details

Name: Sudha Khurana, PhD

Affiliation: Atreca, Inc.

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

Logo

Take Control of Your Skin and Body Changes Today.

Try out Spots for free, set up only takes 2 mins.

spots app storespots app store

Join others from around the world: