Clinical trial · Interventional
AO-176 in Multiple Solid Tumor Malignancies
A Phase 1/2 Multicenter, Open-Label, Dose-Escalation and Dose-Expansion Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics, and Antitumor Activity of AO-176
NCT03834948CI-TRIAL-00068967completedPhase 1 / Phase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This is a first-in-human, Phase 1/2 multi-center, open-label, dose escalation and expansion study of AO-176 which will evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, and clinical effects of AO-176 in patients with advanced solid tumors.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Solid Tumor | Solid Neoplasm | CURATED_BROADER | 0.80 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| AO-176 | Drug | — | UNRESOLVED |
| AO-176 + Paclitaxel | Drug | — | UNRESOLVED |
| AO-176 + Pembrolizumab | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (6)
- type
- EXPERIMENTAL
- label
- AO-176 Dose Escalation
- description
- Each dose escalation cohort will initially recruit 3 patients to receive AO-176 in a standard 3+3 design; cohorts will be expanded in the event of a DLT.
- interventionNames
- Drug: AO-176
- type
- EXPERIMENTAL
- label
- AO-176 Dose Expansion
- description
- Once the MTD/RP2D has been established, tumor-specific dose expansion cohorts will be recruited to further assess safety and evaluate preliminary efficacy of AO-176.
- interventionNames
- Drug: AO-176
- type
- EXPERIMENTAL
- label
- AO-176 + Paclitaxel Dose Escalation
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Key Inclusion Criteria 1. Select advanced solid tumor for which standard therapy proven to provide clinical benefit does not exist, or is no longer effective Part A: * Epithelial ovarian carcinoma (EOC) * Endometrial carcinoma * Castration resistant prostate cancer * Non-small cell lung adenocarcinoma * Papillary thyroid carcinoma * Malignant mesothelioma (pleural or peritoneal) * Gastroesophageal adenocarcinoma * Squamous cell carcinoma of the head and neck Part B and Part C: * Platinum-resistant EOC (including fallopian tube or primary peritoneal cancer) * Endometrial carcinoma * Gastric adenocarcinoma/gastroesophageal adenocarcinoma 2. Measurable disease 3. ECOG status 0-1 4. Resolution of prior-therapy-related adverse effects 5. Minimum of 4 weeks or 5 half-lives since last dose of cancer therapy Key Exclusion Criteria: 1. Previous hypersensitivity reaction to treatment with another monoclonal antibody 2. Unresolved hypersensitivity to paclitaxel or any of its excipients (Part B only). Patients who have been desensitized may participate. 3. Part C Only 1. History of interstitial lung disease or a history of (non-infectious) pneumonitis that required steroids or has current pneumonitis. 2. History of immune mediated colitis, hepatitis, endocrinopathies, nephritis or significant immune mediated skin reactions such as toxic epidermal necrolitis or Stevens -Johnson Syndrome 3. History of any autoimmune disease which required systemic therapy\* in the past 2 years (i.e., with use of disease modifying agents, corticosteroids or immunosuppressive drugs) including but not limited to: i. Inflammatory bowel disease (including ulcerative colitis and Crohn's Disease) ii. Rheumatoid arthritis iii. Systemic progressive sclerosis (scleroderma) iv. Systemic lupus erythematosus v. Autoimmune vasculitis (e.g. Wegener's granulomatosis) \*Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency) is not considered a form of systemic treatment and is allowed) 4. Prior treatment with a checkpoint inhibitor (anti-PD-1, PD-L1, CTLA-4 etc.) within 4 weeks prior to the start of study drug 5. Prior treatment with a CD47-targeted therapy 6. Prior organ or stem cell transplant
References
Publications (1)
- DERIVEDAndrejeva G, Capoccia BJ, Hiebsch RR, Donio MJ, Darwech IM, Puro RJ, Pereira DS. Novel SIRPalpha Antibodies That Induce Single-Agent Phagocytosis of Tumor Cells while Preserving T Cells. J Immunol. 2021 Feb 15;206(4):712-721. doi: 10.4049/jimmunol.2001019. Epub 2021 Jan 11. PMID 33431660