Summary

for people ages 18 years and up (full criteria)
at UCLA
study started
estimated completion

Description

Summary

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.

Official Title

A Phase 1 Multiple-Dose Study to Evaluate the Safety and Tolerability of XmAb®22841 Monotherapy and in Combination With Pembrolizumab in Subjects With Selected Advanced Solid Tumors (DUET-4)

Keywords

Melanoma Cervical Carcinoma Pancreatic Carcinoma Triple Negative Breast Cancer Hepatocellular Carcinoma Urothelial Carcinoma Squamous Cell Carcinoma of the Head and Neck Nasopharyngeal Carcinoma Renal Cell Carcinoma Non-small Cell Lung Carcinoma Small Cell Lung Carcinoma Gastric or Gastroesophageal Junction Adenocarcinoma Advanced or Metastatic Solid Tumors Prostate Carcinoma MSI-H Mismatch Repair Deficiency Epithelial Ovarian Cancer Fallopian Tube Cancer Primary Peritoneal Carcinoma Intrahepatic Cholangiocarcinoma DUET-4 Advanced solid tumors Metastatic solid tumors Cervical Cancer Pancreatic Cancer Hepatocellular/Liver Cancer Urothelial Cancer Renal Cell Cancer Non-small Cell Lung Cancer Small Cell Lung Cancer Gastric Cancer Gastroesophageal Junction Cancer Lymphocyte-activation gene 3 (LAG3) Cytotoxic T-lymphocyte-associated protein 4 (CTLA4) Prostate Cancer MSI (microsatellite instability)-high tumors MMR (mismatch repair)-deficient tumors Carcinoma Carcinoma, Squamous Cell Ovarian Neoplasms Carcinoma, Ovarian Epithelial Fallopian Tube Neoplasms Triple Negative Breast Neoplasms Cholangiocarcinoma Lung Neoplasms Squamous Cell Carcinoma of Head and Neck Carcinoma, Non-Small-Cell Lung Pancreatic Neoplasms Pembrolizumab XmAb®22841 Pembrolizumab (Keytruda®)

Eligibility

You can join if…

Open to people ages 18 years and up

  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:
  5. Melanoma (excluding uveal melanoma)
  6. Cervical carcinoma
  7. Pancreatic carcinoma
  8. Breast carcinoma that is estrogen receptor, progesterone receptor, and Her2 negative (TNBC)
  9. Hepatocellular carcinoma
  10. Urothelial carcinoma
  11. Squamous cell carcinoma of the head and neck (HNSCC)
  12. Nasopharyngeal carcinoma (NPC)
  13. Renal cell carcinoma
  14. . Microsatellite instability-high or mismatch repair deficient tumors
  15. . Small cell lung carcinoma or NSCLC
  16. . Gastric or gastroesophageal junction adenocarcinoma
  17. . Prostate adenocarcinoma
  18. . Epithelial ovarian cancer, fallopian tube cancer, or primary peritoneal cancer
  19. . Intrahepatic cholangiocarcinoma
  20. . Subjects in the combination cohorts in Part A with XmAb22841 and pembrolizumab may have an advanced solid tumor that either:
  21. 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
  22. 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.

You CAN'T join if...

  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, 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.

Locations

  • UCLA Hematology & Oncology Clinic accepting new patients
    Los Angeles California 90095 United States
  • University of Utah, Huntsman Cancer Institute accepting new patients
    Salt Lake City Utah 84112 United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Xencor, Inc.
ID
NCT03849469
Phase
Phase 1
Study Type
Interventional
Last Updated