Clinical Trials
2
Trial Phases
1 Phases
Drug Approvals
0
Drug Approvals
No drug approvals found
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Clinical Trials
Distribution across different clinical trial phases (2 trials with phase data)• Click on a phase to view related trials
A Phase 1 in Patients with HLA-A*0201+ and WT1+ Recurrent/Metastatic Cancers
- Conditions
- Pancreatic CancerColorectal CancerGastric CancerOvarian 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
A Phase 1 Study in Patients with HPV16+ Recurrent/ Metastatic Head and Neck Squamous Cell Carcinoma
- Conditions
- Head and Neck CancerHPV Positive Oropharyngeal Squamous Cell CarcinomaHPV-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
News
BioNTech's BNT113 mRNA Cancer Vaccine Advances in Phase 2 Trial for HPV+ Head and Neck Cancer
BioNTech's BNT113, an mRNA cancer vaccine targeting HPV16+ oncoproteins E6 and E7, is being evaluated in the Phase 2 AHEAD-MERIT trial combined with pembrolizumab versus pembrolizumab alone for unresectable recurrent or metastatic HPV+ head and neck squamous cell carcinoma.
Cue Biopharma Initiates Phase 1b Trial of CUE-102 for Recurrent Glioblastoma at Dana-Farber
Cue Biopharma has dosed the first patient with CUE-102 in a Phase 1b investigator-sponsored trial for recurrent glioblastoma multiforme at Dana-Farber Cancer Institute.
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.