A Study of XmAb®22841 Monotherapy & in Combination w/ Pembrolizumab in Subjects w/ Selected Advanced Solid Tumors

Phase 1

Completed

• Conditions: Triple Negative Breast Cancer; Hepatocellular Carcinoma; Epithelial Ovarian Cancer; Fallopian Tube Cancer; Non-small Cell Lung Carcinoma; Advanced or Metastatic Solid Tumors; Squamous Cell Anal Cancer; Small Cell Lung Carcinoma; Gastric or Gastroesophageal Junction Adenocarcinoma; Squamous Cell Vulvar Carcinoma
• Interventions: Biological: XmAb®22841; Biological: Pembrolizumab (Keytruda®)

• Registration Number: NCT03849469
• Lead Sponsor: Xencor, Inc.

Brief 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.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2019-02-19
• Study First Submitted QC: 2019-02-19
• Study First Posted: 2019-02-21
• Study Start: 2019-05-29
• Primary Completion: 2023-02-16
• Study Completion: 2023-02-16
• Status Verified: 2023-03
• Last Update Submitted: 2023-03-29
• Last Update Posted: 2023-03-30

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 78

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
   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. Colorectal carcinoma or endometrial carcinoma
   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

5. 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:

2. Anti-PD1 refractory melanoma (or any uveal melanoma)

3. Anti-PD1 refractory NSCLC

4. Anti-PD1 refractory renal cell carcinoma (with clear cell component)

5. Anti-PD1 refractory urothelial carcinoma

6. Head and neck squamous cell carcinoma

7. Hepatocellular carcinoma

8. Gastric adenocarcinoma

9. Cervical carcinoma

10. Breast carcinoma that is estrogen receptor, progesterone receptor, and HER2 negative (TNBC)

11. Epithelial ovarian cancer

12. Nasopharyngeal carcinoma

13. Squamous cell anal carcinoma

14. Squamous cell penile carcinoma

15. 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, 4P and 4Pi; 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.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SEQUENTIAL

Arm && Interventions

Group	Intervention	Description
Arm 2	Pembrolizumab (Keytruda®)	Arm 2: Combination of XmAb®22841 and Pembrolizumab (Keytruda®)
Arm 1	XmAb®22841	Arm 1: XmAb®22841 Monotherapy
Arm 2	XmAb®22841	Arm 2: Combination of XmAb®22841 and Pembrolizumab (Keytruda®)

Primary Outcome Measures

Name	Time	Method
Safety and tolerability profile of XmAb22841 assessed by rates of treatment-related adverse events (AEs), graded by CTCAE v4.03.	56 Days	Rates of treatment-related adverse events (AEs), graded by CTCAE v4.03, and additionally categorized as either immune-related or non-immune AEs.

Trial Locations

Locations (28)

Emory University Hospital Midtown; 🇺🇸 Atlanta, Georgia, United States

Winship Cancer Institute, Emory University; 🇺🇸 Atlanta, Georgia, United States

Brigham and Women's Hospital; 🇺🇸 Boston, Massachusetts, United States

Dana-Farber Cancer Institute; 🇺🇸 Boston, Massachusetts, United States

Karmanos Cancer Institute Weisberg Cancer Treatment Center; 🇺🇸 Farmington Hills, Michigan, United States

Hospital of the University of Pennsylvania - Perelman Center for Advanced Medicine; 🇺🇸 Philadelphia, Pennsylvania, United States

UPMC Hillman Cancer Center; 🇺🇸 Pittsburgh, Pennsylvania, United States

Mary Crowley Cancer Research - Medical City; 🇺🇸 Dallas, Texas, United States

The University of Texas MD Anderson Cancer Center; 🇺🇸 Houston, Texas, United States

UCSD Medical Center - Encinitas; 🇺🇸 Encinitas, California, United States

Koman Family Outpatient Pavilion; 🇺🇸 La Jolla, California, United States

UC San Diego Medical Center - La Jolla (Jacobs Medical Center / Thornton Pavilion); 🇺🇸 La Jolla, California, United States

UCSD Altman Clinical and Translational Research Institute Building (ACTRI); 🇺🇸 La Jolla, California, United States

UCSD Perlman Medical Offices; 🇺🇸 La Jolla, California, United States

UC San Diego Moores Cancer Center; 🇺🇸 La Jolla, California, United States

UC San Diego Medical Center - Hillcrest; 🇺🇸 San Diego, California, United States

UCLA Hematology & Oncology Clinic; 🇺🇸 Los Angeles, California, United States

UCSD Rancho Bernardo Medical Office; 🇺🇸 San Diego, California, United States

UCSD Medical Center - Vista; 🇺🇸 Vista, California, United States

University of Iowa Hospital and Clinics; 🇺🇸 Iowa City, Iowa, United States

Brigham and Women's Health Care Center, Chestnut Hill; 🇺🇸 Chestnut Hill, Massachusetts, United States

University of Michigan Medical School; 🇺🇸 Ann Arbor, Michigan, United States

Karmanos Cancer Institute; 🇺🇸 Detroit, Michigan, United States

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

Columbia University Medical Center; 🇺🇸 New York, New York, United States

UPMC Shadyside Hospital; 🇺🇸 Pittsburgh, Pennsylvania, United States

NYU Langone Medical Center (Tisch Hospital); 🇺🇸 New York, New York, United States

University of Utah, Huntsman Cancer Institute; 🇺🇸 Salt Lake City, Utah, United States