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Cue Biopharma, Inc

Cue Biopharma, Inc logo
🇺🇸United States
Ownership
-
Employees
-
Market Cap
$35.4M
Website

Clinical Trials

2

Active:1
Completed:1

Trial Phases

1 Phases

Phase 1:2

Drug Approvals

0

Drug Approvals

No drug approvals found

This company may not have drug approvals in our database

Clinical Trials

Distribution across different clinical trial phases (2 trials with phase data)• Click on a phase to view related trials

Phase 1
2 (100.0%)

A Phase 1 in Patients with HLA-A*0201+ and WT1+ Recurrent/Metastatic Cancers

Phase 1
Completed
Conditions
Pancreatic Cancer
Colorectal Cancer
Gastric Cancer
Ovarian Cancer
Interventions
First Posted Date
2022-05-04
Last Posted Date
2025-03-18
Lead Sponsor
Cue Biopharma
Target Recruit Count
42
Registration Number
NCT05360680
Locations
🇺🇸

Mayo Clinic, Phoenix, Arizona, United States

🇺🇸

Cedars-Sinai Medical Center, Los Angeles, California, United States

🇺🇸

Stanford Advanced Medicine Cancer Center, Palo Alto, California, United States

and more 12 locations

A Phase 1 Study in Patients with HPV16+ Recurrent/ Metastatic Head and Neck Squamous Cell Carcinoma

Phase 1
Active, not recruiting
Conditions
Head and Neck Cancer
HPV Positive Oropharyngeal Squamous Cell Carcinoma
HPV-Related Carcinoma
Interventions
First Posted Date
2019-06-07
Last Posted Date
2025-03-11
Lead Sponsor
Cue Biopharma
Target Recruit Count
85
Registration Number
NCT03978689
Locations
🇺🇸

University of Arizona, Tucson, Arizona, United States

🇺🇸

Stanford University Medical Center, Palo Alto, California, United States

🇺🇸

Yale School of Medicine, New Haven, Connecticut, United States

and more 14 locations

News

CUE-101 Combination Therapy Achieves 50% Response Rate in HPV+ Head and Neck Cancer Trial

Cue Biopharma's CUE-101 combined with pembrolizumab demonstrated a 50% overall response rate in patients with recurrent/metastatic HPV+ head and neck squamous cell carcinoma, significantly outperforming historical pembrolizumab monotherapy data.

Cue Biopharma Receives Positive FDA Feedback for CUE-401 Autoimmune Therapy, Advances Toward IND Filing

Cue Biopharma received positive Pre-IND feedback from the FDA for CUE-401, a first-in-class bispecific fusion protein designed to treat autoimmune diseases by inducing regulatory T cells.

Boehringer Ingelheim and Cue Biopharma Partner on Novel B Cell-Targeting Therapy for Autoimmune Diseases

Boehringer Ingelheim and Cue Biopharma have formed a strategic partnership to develop CUE-501, a first-in-class bispecific therapy designed to selectively deplete disease-causing B cells in autoimmune conditions.

Cue Biopharma's CUE-101 and CUE-102 Show Promise in Phase 1 Trials for Head and Neck and WT1-Positive Cancers

CUE-101 combined with pembrolizumab demonstrates a 46% objective response rate and a 91.3% 12-month overall survival rate in first-line HPV+ R/M HNSCC patients.

Cue Biopharma's CUE-101 and CUE-102 Show Promising Phase 1 Results in Cancer Trials

Cue Biopharma's CUE-101, combined with pembrolizumab, demonstrated a 46% objective response rate and a 91.3% 12-month overall survival rate in head and neck cancer patients.

Cue Biopharma Announces Positive Phase 1 Data for CUE-101 and CUE-102 at SITC 2024

CUE-101 combined with pembrolizumab shows a 46% objective response rate and 91.3% 12-month overall survival in first-line HPV+ recurrent/metastatic head and neck squamous cell carcinoma patients.

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