Cross Indication Research

Our approach:

Exploring indication spaces for targets and compounds, for new ideas as well as for shelved projects or even for established drugs.

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Whether First Positioning Or Repurposing – We Can Support You

We assess the specific indication option space for your asset using big data analysis tools. We propose first positioning, indication expansion, repositioning, or repurposing building on our more than 10 years of experience. We identify the most suited proof-of-concept indication for your asset. We propose feasible paths forward by identifying the most translational in vivo or ex vivo models for your selected indication. We have as well a broad track record of projects that found their home in oftentimes unexpected indications. We perform in silico-, in vivo-, ex vivo-, and in vitro-studies for you in our labs - or we orchestrate your studies with third partners. We assist you from conceptual drafting to clinical translation and regulatory documentation by de-risking every step.

How Cross Indication Research Works

We offer in silico analyses including broad literature and patent review in a first screening approach and in-depth assessments of selected indications. Text mining, signaling pathway- and mode-of-action analyses are used to figure out the most compelling scientific rationale for optimal positioning of your asset in the disease landscape.

Availability assessment of preclinical models and their translatability into the clinical situation will guide you to the right path forward. We help you to rigorously assess your asset by head to head comparison with standard of care medications and competitor pipeline compounds.

We build on our long-term experience in a wide variety of pharmacodynamic or disease models from various fields of indications such as

  • inflammation and autoimmunity (e.g. mouse and rat models of rheumatoid arthritis inflammatory skin diseases, inflammatory bowel diseases, Lupus nephritis)
  • fibrotic diseases (e.g. NASH, liver fibrosis and liver cirrhosis models)
  • urogenital disease models (e.g. models for overactive bladder, interstitial cystitis/bladder pain syndrome or benign prostate hyperplasia)
  • neurologic disease models (e.g. models for brain edema, ischemic stroke, or traumatic brain injury)
  • pain models (e.g. diabetic and surgical models of neuropathic pain)

We smartly combine our in-house disease model repertoire with external model expertise to guarantee you outstanding preclinical de-risking programs for your asset.

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Our Services & Solutions along
the Drug Development Value Chain

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Discovery

Preclinical

Clinical Phase I

Clinical Phase II

Overall Services

NUVISAN Overall Services along the Value Chain

API Manufacturig
(Non-GMP / GMP)

Formulation
Development

Pharmaceutical
Analysis

Bioanalysis
(Discovery and Regulated)

Biomarkers
(exploratory & GxP)

Translational
Pharmacology

Healthy Volunteers
& Patient Studies

Clinical Trial
Supplies

Regulatory
Affairs

Backend
Services

Corporate Project
Management

NUVISAN Overall Services along the Value Chain

API Manufacturig
(Non-GMP / GMP)

Formulation
Development

Pharmaceutical
Analysis

Bioanalysis
(Discovery and Regulated)

Biomarkers
(exploratory & GxP)

Translational
Pharmacology

Healthy Volunteers
& Patient Studies

Clinical Trial
Supplies

Regulatory
Affairs

Backend
Services

Corporate Project
Management

NUVISAN Overall Services along the Value Chain

API Manufacturig
(Non-GMP / GMP)

Formulation
Development

Pharmaceutical
Analysis

Bioanalysis
(Discovery and Regulated)

Biomarkers
(exploratory & GxP)

Translational
Pharmacology

Healthy Volunteers
& Patient Studies

Clinical Trial
Supplies

Regulatory
Affairs

Backend
Services

Corporate Project
Management

NUVISAN Overall Services along the Value Chain

API Manufacturig
(Non-GMP / GMP)

Formulation
Development

Pharmaceutical
Analysis

Bioanalysis
(Discovery and Regulated)

Biomarkers
(exploratory & GxP)

Translational
Pharmacology

Healthy Volunteers
& Patient Studies

Clinical Trial
Supplies

Regulatory
Affairs

Backend
Services

Corporate Project
Management

NUVISAN Overall Services along the Value Chain

API Manufacturig
(Non-GMP / GMP)

Formulation
Development

Pharmaceutical
Analysis

Bioanalysis
(Discovery and Regulated)

Biomarkers
(exploratory & GxP)

Translational
Pharmacology

Healthy Volunteers
& Patient Studies

Clinical Trial
Supplies

Regulatory
Affairs

Backend
Services

Corporate Project
Management

NUVISAN Overall Services along the Value Chain

API Manufacturig
(Non-GMP / GMP)

Formulation
Development

Pharmaceutical
Analysis

Bioanalysis
(Discovery and Regulated)

Biomarkers
(exploratory & GxP)

Translational
Pharmacology

Healthy Volunteers
& Patient Studies

Clinical Trial
Supplies

Regulatory
Affairs

Backend
Services

Corporate Project
Management