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Accelerating Pancreatic Cancer Drug Development

Pancreatic cancer presents one of the most formidable challenges in oncology, characterized by late diagnosis, aggressive progression, and limited therapeutic options. Alfa Cytology stands at the forefront of preclinical drug development, specializing in innovative solutions for Cancer, pancreas therapeutics. Leveraging deep scientific expertise, Alfa Cytology delivers a comprehensive suite of preclinical services encompassing target validation, lead optimization, pharmacology, toxicology, and IND-enabling studies. Our integrated approach combines advanced in vitro and in vivo platforms with robust biomarker analysis and translational models tailored specifically for pancreatic cancer research. Alfa Cytology’s team of experienced scientists ensures that every stage of development adheres to the highest standards of scientific rigor and regulatory compliance, facilitating a seamless transition from discovery to clinical readiness. By uniting state-of-the-art technologies with a strong commitment to quality and precision, Alfa Cytology accelerates the path to therapeutic breakthroughs. Our mission is to empower biopharmaceutical partners to advance novel Cancer, pancreas therapies with confidence and efficiency, ultimately improving patient outcomes in this critical area of unmet medical need.

What is Pancreatic CancerTargets for Pancreatic CancerDrug Discovery and Development ServicesWhy Choose Us

What is Pancreatic Cancer

Pancreatic cancer is a highly aggressive malignancy arising from the pancreas, an organ crucial for digestion and blood sugar regulation. The majority of cases originate from the exocrine ducts (pancreatic ductal adenocarcinoma), while less common types include neuroendocrine tumors, acinar cell carcinoma, and rare pediatric forms like pancreatoblastoma. The disease develops through a series of genetic and epigenetic changes, commonly involving mutations in KRAS and TP53 genes, as well as disruptions in key cellular signaling pathways. Risk factors include chronic pancreatitis, smoking, obesity, diabetes, and hereditary syndromes such as BRCA mutations. Pancreatic cancer is notorious for its rapid local invasion, early spread to distant organs, and a dense stromal environment that limits treatment effectiveness. Clinically, patients often present late with symptoms such as unexplained weight loss, abdominal pain, jaundice, and new-onset diabetes, leading to a poor prognosis and high mortality. Diagnosis is based on clinical assessment, laboratory markers (e.g., CA 19-9), and imaging studies like CT and MRI, with histological confirmation via biopsy. Treatment options are limited and depend on cancer type and stage, including surgery, chemotherapy (e.g., liposomal irinotecan, nab-paclitaxel), targeted therapies (e.g., olaparib, sunitinib, everolimus), and, in some cases, radiotherapy. Despite advances, the five-year survival rate remains low due to late detection and resistance to therapy.

Launched Drugs

Structure Generic Name CAS Registry Number Molecular Formula Molecular Weight
irinotecan hydrochloride liposome injection; irinotecan liposome injection
belzutifan (Rec INN; USAN) 1672668-24-4 C17 H12 F3 N O4 S 383.342
sulfatinib; surufatinib (Rec INN; USAN) 1308672-74-3 C24 H28 N6 O3 S 480.583
Irinotecan sucrosofate; liposome irinotecan injection; nanoliposomal irinotecan sucrosofate
olaparib (Rec INN; USAN) 763113-22-0 C24 H23 F N4 O3 434.463
cabozantinib S-malate (Prop INNM; USAN) 1140909-48-3; 849217-68-1 (free base) C28 H24 F N3 O5 . C4 H6 O5 635.593
sunitinib malate (Rec INNM; USAN) 341031-54-7; 557795-19-4 (free base) C22 H27 F N4 O2 . C4 H6 O5 532.561
nab-paclitaxel; paclitaxel nanoparticles
erlotinib hydrochloride (Rec INNM; USAN) 183319-69-9; 183321-74-6 (free base) C22 H23 N3 O4 . Cl H 429.897
everolimus (Rec INN; USAN) 159351-69-6 C53 H83 N O14 958.224

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Targets for Pancreatic Cancer

Targets in Clinical or Later Phases of Development

Target Name Gene Symbol
dihydropyrimidine dehydrogenase DPYD
DNA topoisomerase I TOP1
epidermal growth factor receptor EGFR
Ribonucleoside-diphosphate reductase
receptor interacting serine/threonine kinase 2 RIPK2
poly(ADP-ribose) polymerase 2 PARP2
poly(ADP-ribose) polymerase 1 PARP1
poly(ADP-ribose) polymerase family member 3 PARP3
thymidylate synthetase TYMS
Tubulin

Pancreatic cancer is characterized by the dysregulation of multiple molecular targets that underpin tumor growth, survival, and immune evasion. Key targets include the epidermal growth factor receptor (EGFR), which drives oncogenic signaling and cell proliferation through activation of pathways such as RAS-RAF-MEK-ERK and PI3K-AKT. Enzymes involved in nucleotide metabolism and DNA synthesis, like thymidylate synthetase (TYMS), dihydrofolate reductase (DHFR), DNA topoisomerase I (TOP1), and uridine monophosphate synthetase (UMPS), support the rapid DNA replication required for tumor expansion and are directly targeted by chemotherapeutic agents. Additionally, poly(ADP-ribose) polymerase 1 (PARP1) plays a crucial role in DNA repair, especially in tumors with homologous recombination deficiencies. The immune checkpoint protein PD-1 (PDCD1) is also significant, as its interaction with PD-L1/PD-L2 suppresses anti-tumor immune responses, facilitating immune escape in pancreatic tumors.

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Drug Discovery and Development Services

In Vitro Efficacy Testing ServicesIn Vivo Model DevelopmentPK/PD Study ServicesIn Vivo Toxicity Assessment ServicesBiomarker Analysis Services

Our In Vitro Efficacy Testing Service accelerates pancreatic cancer drug discovery by providing robust, sensitive platforms for screening compounds, biologics, and immunotherapies. We evaluate key targets including PARP, PD-1/PD-L1, EGFR, and somatostatin receptors using advanced biochemical, cell-based, and biophysical assays. Employing methods such as ATP, chemiluminescence, flow cytometry, FACS, and surface plasmon resonance, we deliver precise measurements of potency, affinity, and efficacy (IC-50, EC-50, Kd, pEC-50). Our comprehensive profiling of drug candidates supports lead optimization, risk assessment, and effective selection, driving development of innovative therapies for pancreatic cancer.

Dna Topoisomerase I Epidermal Growth Factor Receptor
Poly(Adp-Ribose) Polymerase 1 Poly(Adp-Ribose) Polymerase 2
Poly(Adp-Ribose) Polymerase Family Member 3 Programmed Cell Death 1
Receptor Interacting Serine/Threonine Kinase 2 Somatostatin Receptor 2
Somatostatin Receptor 3

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Why Choose Us

Choosing Alfa Cytology means partnering with a team that is deeply committed to advancing the field of Cancer, pancreas therapeutics. At Alfa Cytology, we specialize in preclinical drug development for Cancer, pancreas, combining in-depth scientific expertise with years of experience in this challenging area. Our professional teams are composed of leading scientists and technical experts who utilize advanced technology platforms to deliver reliable and innovative solutions tailored to your research needs. Alfa Cytology has a proven track record of supporting clients through every stage of preclinical development, consistently delivering high-quality results that meet the most stringent industry standards. We adhere strictly to regulatory requirements and maintain rigorous quality control processes to ensure the integrity and reproducibility of our data. Above all, Alfa Cytology is dedicated to making a meaningful impact in the fight against Cancer, pancreas by supporting the development of novel therapeutics. Our commitment to professionalism, reliability, and scientific excellence makes Alfa Cytology the trusted choice for your preclinical drug development needs.

FAQs for Our Services

Q: What are the main preclinical research challenges specific to developing drugs for pancreatic cancer?

A: Pancreatic cancer presents unique preclinical research challenges, including the aggressive nature of the disease, late diagnosis, and poor prognosis. The pancreatic tumor microenvironment is highly desmoplastic, which limits drug penetration and efficacy. Additionally, there is a lack of reliable and predictive animal models that fully recapitulate human pancreatic cancer biology. Our company addresses these challenges by utilizing advanced 3D cell culture systems, patient-derived xenograft (PDX) models, and genetically engineered mouse models to better mimic the human disease and improve translational relevance.

Q: What are the key regulatory considerations for preclinical drug development targeting pancreatic cancer?

A: Regulatory agencies such as the FDA and EMA require robust preclinical data to support the safety and efficacy of new drug candidates. For pancreatic cancer, it is essential to demonstrate pharmacokinetic and pharmacodynamic profiles, dose-ranging studies, and toxicology assessments in relevant models. Special attention must be paid to off-target effects and the potential for pancreatic toxicity. Our preclinical services are designed to meet or exceed regulatory expectations, providing comprehensive data packages and regulatory documentation to facilitate smooth IND/CTA submissions.

Q: What are the technical aspects that should be considered in preclinical research for pancreatic cancer therapeutics?

A: Technical considerations include the selection of appropriate in vitro and in vivo models, development of reliable biomarkers for efficacy and toxicity, and the use of advanced imaging and analytical techniques. It is also crucial to assess drug delivery mechanisms due to the dense stroma in pancreatic tumors. Our team leverages state-of-the-art technologies such as high-content imaging, next-generation sequencing, and multiplex biomarker analysis to provide detailed mechanistic insights and optimize candidate selection.

Q: What is the typical timeline and cost for preclinical development of a pancreatic cancer drug candidate?

A: The preclinical development phase for pancreatic cancer therapeutics typically ranges from 18 to 36 months, depending on the complexity of the program and the number of studies required. Costs can vary significantly, but a comprehensive preclinical package—including efficacy, safety, pharmacokinetics, and regulatory support—can range from $2 million to $6 million. We offer flexible, milestone-driven project management and transparent budgeting to help our clients plan and allocate resources efficiently.

Q: What are the critical success factors in preclinical drug development for pancreatic cancer?

A: Success in preclinical development for pancreatic cancer relies on several factors: the use of disease-relevant models, early identification of pharmacodynamic biomarkers, rigorous safety and efficacy assessment, and strong regulatory strategy. Collaboration between multidisciplinary teams and early engagement with regulatory authorities also play a vital role. Our company’s integrated approach ensures that scientific, technical, and regulatory aspects are aligned from the outset, increasing the likelihood of successful clinical translation.

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