Adenoid cystic carcinoma (ACC) is a rare, slow-growing malignant tumour arising from salivary glands and other secretory tissues. According to Yu-Ting Yin et al., 2025, ACC represents approximately 1.5-2% of all head and neck cancers. Current therapies include surgery, radiotherapy, and systemic treatments, but the growing focus is on targeted agents (such as those acting on the MYB/NFIB fusion or Notch pathway) and immunotherapy driven by biomarker-led strategies. According to the adenoid cystic carcinoma pipeline analysis by Expert Market Research, the pipeline is expanding significantly, and this is expected to drive substantial growth in treatment options over the coming years.
Major companies involved in the adenoid cystic carcinoma pipeline analysis include Rgenta Therapeutics Inc., Cellestia Biotech AG, and others.
Leading drugs currently in the pipeline include CB-103, RGT-61159, and others.
The pipeline is expanding with advancements in targeted therapies, immunotherapies, and precision medicine, driving stronger clinical progress and diversified treatment options in the coming years.
The Adenoid Cystic Carcinoma Pipeline Analysis Report by Expert Market Research gives comprehensive insights into adenoid cystic carcinoma therapeutics currently undergoing clinical trials. It covers various aspects related to the details of each of these drugs under development for adenoid cystic carcinoma. The adenoid cystic carcinoma report assessment includes the analysis of over 100 pipeline drugs and 50+ companies. The adenoid cystic carcinoma pipeline landscape will include an analysis based on efficacy and safety measure outcomes published for the trials, including their adverse effects on patients suffering from the condition, and alignment with adenoid cystic carcinoma treatment guidelines to ensure optimal care practices.
The assessment part will include a detailed analysis of each drug, drug class, clinical studies, phase type, drug type, route of administration, and ongoing product development activities related to adenoid cystic carcinoma.
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Adenoid cystic carcinoma (ACC) is a rare, slow-growing cancer that typically develops in the salivary glands but can also occur in other glandular tissues. It arises due to genetic mutations that lead to the overexpression of the MYB oncogene, causing uncontrolled cell proliferation and tumor formation. ACC often spreads along nerves and can metastasize to distant organs.
Adenoid cystic carcinoma treatment involves surgical removal of the tumor followed by radiation therapy to prevent recurrence. Chemotherapy or targeted therapies may be used for advanced or metastatic cases. In September 2025, Rgenta Therapeutics received Orphan Drug Designation from the U.S. Food and Drug Administration for RGT-61159, an oral small molecule inhibitor targeting the MYB oncogene. The drug is being evaluated in a Phase 1a/b clinical trial for patients with advanced, relapsed, or refractory ACC, aiming to offer a novel therapeutic option for this rare malignancy.
According to Yu-Ting Yin et al. (2025), adenoid cystic carcinoma (ACC) represents approximately 1.5–2% of all head and neck cancers. It is known for its aggressive nature, frequent recurrence, and distant metastases occurring in 35–50% of cases, leading to a poor long-term survival rate. As per the Cleveland Clinic, around 1,200 individuals in the United States are diagnosed with ACC annually, with the majority aged between 40 and 60 years. Ongoing epidemiological studies continue to refine incidence patterns and disease outcomes.
This section of the report covers the analysis of adenoid cystic carcinoma drug candidates based on several segmentations, including:
By Phase
The pipeline assessment report covers 50+ drug analyses based on phase:
By Drug Class
The adenoid cystic carcinoma pipeline analysis report covers 50+ drug analyses based on drug classes:
By Route of Administration
The pipeline assessment report covers 50+ drug analyses based on the route of administration.
The report covers phase I, phase II, phase III, phase IV, and early-phase drugs. The coverage includes an in-depth analysis of each drug across these phases. According to EMR analysis, phase II covers a major share of the total adenoid cystic carcinoma clinical trials, at 50%. It is followed by Phase I with 50%. The active developments in Phase I and Phase II indicate promising advancements in the pipeline, potentially accelerating future treatment innovations and market growth.
The drug molecule categories covered under the adenoid cystic carcinoma pipeline analysis include small molecules, oligonucleotides, and peptides. The adenoid cystic carcinoma report provides a comparative analysis of the drug classes for each drug in various phases of clinical trials for adenoid cystic carcinoma. Immune checkpoint inhibitors targeting B7-H4 are emerging as a novel drug class in the adenoid cystic carcinoma (ACC) treatment pipeline. For instance, AZD8205, an investigational therapy, specifically blocks B7-H4 to restore immune activity against tumor cells. Preclinical studies have shown promising tumor regression in B7-H4–expressing ACC, highlighting its potential as a targeted and personalized treatment approach.
The EMR report for the adenoid cystic carcinoma pipeline covers the profile of key companies involved in clinical trials and their drugs under development. It provides a detailed adenoid cystic carcinoma therapeutic assessment, analyzing the competitive dynamics of the clinical trial landscape. Below is the list of a few players involved in adenoid cystic carcinoma clinical trials:
This section covers the detailed analysis of each drug under multiple phases, including phase I, phase II, phase III, phase IV, and emerging drugs for adenoid cystic carcinoma. It includes product description, trial ID, study type, drug class, mode of administration, and recruitment status of adenoid cystic carcinoma drug candidates.
CB-103 is an oral pan-NOTCH pathway inhibitor being evaluated in combination with either Lenvatinib or Abemaciclib for patients with NOTCH-activated adenoid cystic carcinoma (ACC). Sponsored and supported by Cellestia Biotech AG, this Phase 1/2 study is examining the drug’s ability to slow tumor progression and enhance survival outcomes. CB-103 targets the NOTCH intracellular domain, aiming to inhibit tumor growth in advanced, metastatic, or recurrent ACC cases.
RGT-61159, developed by Rgenta Therapeutics Inc., is an oral small-molecule MYB inhibitor currently being evaluated in a Phase 1 clinical study for adults with relapsed or refractory adenoid cystic carcinoma (ACC) or colorectal carcinoma (CRC). The study is assessing the drug’s safety, tolerability, and anti-tumor activity. RGT-61159 functions as an mRNA degrader that reduces MYB mRNA and protein levels, potentially slowing or halting cancer cell growth and progression.
*Please note that this is only a partial list; the complete list of drugs will be available in the full report.*
The Adenoid Cystic Carcinoma Pipeline Analysis Report provides a strategic overview of the latest and future landscape of treatments for adenoid cystic carcinoma. It provides necessary information for making informed investment decisions along with research, development, and strategic planning efforts. The stakeholders will benefit from the essential insights into adenoid cystic carcinoma collaborations, regulatory environments, and potential growth opportunities.
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*While we strive to always give you current and accurate information, the numbers depicted on the website are indicative and may differ from the actual numbers in the main report. At Expert Market Research, we aim to bring you the latest insights and trends in the market. Using our analyses and forecasts, stakeholders can understand the market dynamics, navigate challenges, and capitalize on opportunities to make data-driven strategic decisions.*
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