This is a Phase 1, multiple dose, ascending-dose escalation study and expansion study designed to define a maximum tolerated dose and/or recommended dose of XmAb22841 monotherapy and in combination with pembrolizumab; to assess safety, tolerability, pharmacokinetics, immunogenicity, and anti-tumor activity of XmAb22841 monotherapy and in combination with pembrolizumab in subjects with select advanced solid tumors.
Overal Status | Start Date | Phase | Study Type |
---|---|---|---|
Recruiting | May 29, 2019 | Phase 1 | Interventional |
Primary Outcome 1 - Measure: Safety and tolerability profile of XmAb22841 assessed by rates of treatment-related adverse events (AEs), graded by CTCAE v4.03.
Primary Outcome 1 - Time Frame: 56 Days
Criteria:
Inclusion Criteria:
PART A (Dose Escalation Cohorts)
1. All subjects' cancer must have progressed after treatment with all available therapies
that are known to confer clinical benefit, or are intolerant to treatment, or refuse
standard treatment.
2. All subjects must have adequate archival tumor, or give consent to a fresh tumor
biopsy.
3. Subjects have an ECOG performance status of 0-1.
4. Subjects in monotherapy and combination therapy cohorts must have histologically or
cytologically confirmed advanced or metastatic solid tumors, including the following:
1. Melanoma (excluding uveal melanoma)
2. Cervical carcinoma
3. Pancreatic carcinoma
4. Breast carcinoma that is estrogen receptor, progesterone receptor, and Her2
negative (TNBC)
5. Hepatocellular carcinoma
6. Urothelial carcinoma
7. Squamous cell carcinoma of the head and neck (HNSCC)
8. Nasopharyngeal carcinoma (NPC)
9. Renal cell carcinoma
10. Microsatellite instability-high or mismatch repair deficient tumors
11. Small cell lung carcinoma or NSCLC
12. Gastric or gastroesophageal junction adenocarcinoma
13. Prostate adenocarcinoma
14. Epithelial ovarian cancer, fallopian tube cancer, or primary peritoneal cancer
15. Intrahepatic cholangiocarcinoma
16. Subjects in the combination cohorts in Part A with XmAb22841 and pembrolizumab
may have an advanced solid tumor that either:
- has progressed after treatment with all available therapies that are known
to confer clinical benefit, or is intolerant or has refused standard
treatment (as for the XmAb22841 monotherapy cohorts), or
- is of a tumor type for which pembrolizumab is an approved indication and has
not previously been treated with an agent targeting PD1 or PDL1.
PART B (Dose Expansion Cohorts)
XmAb22841 Single Agent Cohort
1. Must have histologically or cytologically confirmed advanced or metastatic solid tumor
that has progressed after treatment with all available therapies that are known to confer
clinical benefit, or are intolerant to treatment, or refuse standard treatment. Eligible
tumor types include the following:
1. Anti-PD1 refractory melanoma (or any uveal melanoma)
2. Anti-PD1 refractory NSCLC
3. Anti-PD1 refractory renal cell carcinoma (with clear cell component)
4. Anti-PD1 refractory urothelial carcinoma
5. Head and neck squamous cell carcinoma
6. Hepatocellular carcinoma
7. Gastric adenocarcinoma
8. Cervical carcinoma
9. Breast carcinoma that is estrogen receptor, progesterone receptor, and HER2 negative
(TNBC)
10. Epithelial ovarian cancer
11. Nasopharyngeal carcinoma
12. Squamous cell anal carcinoma
13. Squamous cell penile carcinoma
14. Squamous cell vulvar carcinoma
XmAb22841 + Pembrolizumab Cohorts
1. Anti-PD-1 refractory melanoma (excluding uveal melanoma)
2. Anti-PD-1 naïve melanoma (excluding uveal melanoma)
3. Anti-PD-1 refractory NSCLC
4. Anti-PD1 naïve NSCLC
a. Must be PD-L1 high (TPS ≥ 50%), with no EGFR or ALK aberrations
5. Anti-PD1 naïve urothelial carcinoma
1. Must be PDL1 positive (CPS of ≥ 10), or ineligible for any platinum-containing
chemotherapy regardless of PDL1 status; or
2. Had disease progression within 12 months of neoadjuvant or adjuvant treatment
with platinum-containing chemotherapy
Exclusion Criteria:
1. Prior treatment with an investigational anti-LAG3 therapy.
2. Treatment with any CTLA4 antibody within 16 weeks of the start of study drug for
Cohorts 1M, 2M, 3M, 1P, and 2P; within 8 weeks for Cohorts 4M, 5M, 3P, and 4P; and
within 3 weeks for Cohorts 6M, 7Mi, 7M, 5P, and 6P.
3. Systemic antineoplastic therapy, unconjugated antibody therapy within 4 weeks of the
first dose of study treatment; or radiotherapy within 2 weeks of the first dose of
study treatment; or small molecule kinase inhibitors within 6 elimination half-lives
of the first dose of study treatment.
4. Have received prior therapy with an anti-PD1, anti-PDL1, or anti PDL2 agent or with an
agent directed to another stimulatory or co-inhibitory T-cell receptor (eg, CTLA4, OX
40, CD137) AND were permanently discontinued from that treatment due to an irAE.
5. Failure to recover from any irAE from prior cancer therapy to Grade ≤ 1.
6. Failure to recover from any other toxicity (other than immune-related toxicity)
related to previous anticancer treatment to Grade ≤ 2.
7. Active known or suspected autoimmune disease (except that subjects are permitted to
enroll if they have vitiligo; type 1 diabetes mellitus; residual hypothyroidism due to
an autoimmune condition that is treatable with hormone replacement therapy only;
psoriasis, atopic dermatitis, or another autoimmune skin condition that is managed
without systemic therapy; or arthritis that is managed without systemic therapy beyond
oral acetaminophen and non-steroidal anti-inflammatory drugs).
8. Receipt of an organ allograft.
9. Treatment with antibiotics within 14 days prior to first dose of study drug.
10. Participants with known HIV.
11. Participants with known chronic hepatitis B virus (HBV) infection treated for less
than 3 months prior to study enrollment and/or with a detectable HBV viral load; or
hepatitis C virus (HCV) infection that has been treated for less than 4 weeks prior to
study enrollment and/or with a detectable HCV viral load; or active HBV/HCV
coinfection.
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Gender: All
Minimum Age: 18 Years
Maximum Age: N/A
Healthy Volunteers: No
Name: Benjamin Thompson, MD, PhD
Role: Study Director
Affiliation: Xencor, Inc.
Name: Benjamin Thompson, MD, PhD
Phone: 858-480-3133
Email: bthompson@xencor.com
Facility | Status | Contact |
---|---|---|
UCSD Medical Center - Encinitas Encinitas, California 92024 United States |
Recruiting | |
Koman Family Outpatient Pavilion La Jolla, California 92037 United States |
Recruiting | |
UC San Diego Medical Center - La Jolla (Jacobs Medical Center / Thornton Pavilion) La Jolla, California 92037 United States |
Recruiting | |
UCSD Altman Clinical and Translational Research Institute Building (ACTRI) La Jolla, California 92037 United States |
Recruiting | |
UCSD Perlman Medical Offices La Jolla, California 92037 United States |
Recruiting | |
UC San Diego Moores Cancer Center La Jolla, California 92093 United States |
Recruiting | |
UCLA Hematology & Oncology Clinic Los Angeles, California 90095 United States |
Recruiting | |
UC San Diego Medical Center - Hillcrest San Diego, California 92103 United States |
Recruiting | |
UCSD Rancho Bernardo Medical Office San Diego, California 92127 United States |
Recruiting | |
UCSD Medical Center - Vista Vista, California 92081 United States |
Recruiting | |
Emory University Hospital Midtown Atlanta, Georgia 30308 United States |
Recruiting | |
Winship Cancer Institute, Emory University Atlanta, Georgia 30322 United States |
Recruiting | |
Brigham and Women's Hospital Boston, Massachusetts 02115 United States |
Recruiting | |
Dana-Farber Cancer Institute Boston, Massachusetts 02215 United States |
Recruiting | |
Brigham and Women's Health Care Center, Chestnut Hill Chestnut Hill, Massachusetts 02467 United States |
Recruiting | |
Karmanos Cancer Institute Detroit, Michigan 48201 United States |
Recruiting | |
Karmanos Cancer Institute Weisberg Cancer Treatment Center Farmington Hills, Michigan 48334 United States |
Recruiting | |
Siteman Cancer Center - West County Creve Coeur, Missouri 63141 United States |
Active, not recruiting | |
Barnes-Jewish Hospital Saint Louis, Missouri 63110 United States |
Active, not recruiting | |
Washington University School of Medicine - Siteman Cancer Center Saint Louis, Missouri 63110 United States |
Active, not recruiting | |
Siteman Cancer Center - South County Saint Louis, Missouri 63129 United States |
Active, not recruiting | |
Siteman Cancer Center - North County Saint Louis, Missouri 63136 United States |
Active, not recruiting | |
Siteman Cancer Center - St. Peters Saint Peters, Missouri 63376 United States |
Active, not recruiting | |
Columbia University Medical Center New York, New York 10032 United States |
Recruiting | |
Hospital of the University of Pennsylvania - Perelman Center for Advanced Medicine Philadelphia, Pennsylvania 19104 United States |
Recruiting | |
UPMC Hillman Cancer Center Pittsburgh, Pennsylvania 15232 United States |
Recruiting | |
UPMC Shadyside Hospital Pittsburgh, Pennsylvania 15232 United States |
Recruiting | |
Mary Crowley Cancer Research - Medical City Dallas, Texas 75230 United States |
Recruiting | |
The University of Texas MD Anderson Cancer Center Houston, Texas 77030 United States |
Recruiting | |
University of Utah, Huntsman Cancer Institute Salt Lake City, Utah 84112 United States |
Recruiting |