Unveiling the Journey: From Drug Discovery to Clinical Trials

18 Apr

The realm of modern medicine owes its groundbreaking advancements to the rigorous process of drug discovery and clinical trials. At the heart of healthcare innovation lies an intricate journey, where scientific inquiry, relentless dedication, and cutting-edge technology converge to shape the future of treatment.

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Drug Discovery:

The quest for new medications begins in the realm of drug discovery, a multidisciplinary domain of biology, chemistry, pharmacology, and computational sciences. The primary goal is to identify and develop compounds that possess therapeutic potential.

Researchers embark on an explorative journey, screening thousands, if not millions, of chemical compounds, searching for molecules that exhibit specific biological activities. This phase involves high-throughput screening, where automated systems test numerous compounds for their ability to interact with a particular biological target, often a protein associated with a disease.

Once promising compounds are identified, the focus shifts to optimising their properties to enhance efficacy and safety. Medicinal chemists work precisely, fine-tuning molecular structures through modifications to improve the compound’s potency and reduce potential side effects.

Validation and Preclinical Studies:

Before human trials, the selected compounds undergo extensive preclinical testing. These studies involve in vitro and in vivo experiments, aiming to understand the compound’s pharmacokinetics (what the body does to a drug), toxicity profile, and efficacy in animal models. This phase provides crucial insights and forms the foundation for subsequent clinical trials.

Clinical Trials:

Armed with convincing preclinical data, promising drug candidates proceed to the pivotal stage of clinical trials—a thoroughly planned and regulated process designed to evaluate a drug's safety and efficacy in humans. Clinical trials are typically conducted over 3 phases.

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Phase I: Safety Assessment:

In Phase I trials, a small group of healthy volunteers receives the investigational drug to assess its safety, dosage range, and potential side effects. The primary focus here is on establishing the drug's safety profile and determining the most suitable dosage for further studies.

Phase II: Efficacy and Safety in Patients:

Phase II trials involve a larger group of patients who have the targeted disease or condition. These trials aim to evaluate the drug’s effectiveness against the specific disease, while continuing to assess its safety and side effects.

Phase III: Confirmation and Regulatory Approval:

Phase III trials incorporate an expanded patient population, providing further evidence of a drug's efficacy, monitoring side effects, and comparing it to existing treatments. The data generated in this phase is crucial for regulatory submissions seeking approval for marketing the drug.

The journey from drug discovery to clinical trials is a sophisticated yet collaborative effort involving scientists, clinicians, regulatory bodies, and patients. It represents the pinnacle of scientific innovation and perseverance, bringing hope to millions by delivering new therapies that improve and save lives.

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Exciting News: Unveiling Our Cutting-edge Clinical Trials Facility in Canary Wharf, London!

We are thrilled to announce the completion of Phase 1 of our first clinical trials facility in the heart of Canary Wharf, London. At the forefront of this groundbreaking endeavour is our client, a world-renowned specialist contract research organization (CRO) and the global leader in conducting human challenge clinical trials for infectious and respiratory disease vaccines and therapeutics. They offer end-to-end early clinical development services to four of the top ten largest global biopharmaceutical companies.

The Bulb team is engaged wholeheartedly in the design and delivery process of this fast track project, showcasing our commitment to excellence in every detail. Our contribution encompasses the creation of a 50-bedroom environmentally controlled floor for volunteers, cutting-edge containment level 2 & 3 laboratories, as well as thoughtfully designed offices and collaboration areas.

Stay tuned for the forthcoming release of our comprehensive case study, complete with captivating photos that offer a glimpse into the sophistication and innovation embedded in the facility.

At Bulb, part of Unispace Life Sciences, our specialists can help in understanding and meeting your laboratory requirements. Get in touch today on 0118 988 9200 or 

Ravi Kalsi

Laboratory Specialist

07719 064995

Get in touch

Ravi Kalsi

Benching

Laboratory benching forms a central part of any laboratory and procuring the laboratory benching to suit your equipment needs and budget is important to us.

If you prefer fixed, robust benching or modular benching that offers flexibility and reconfiguration, our laboratory furniture manufacturers can deliver the perfect solution.

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Worktops

Depending on your research focus your worktop design requirements might change to allow:

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Trespa Toplab Base is the industry favourite, but we can offer alternative worktops such as Corian, Stainless Steel, Epoxy Resin, Hardwood, Phenolic Resin to match your needs.

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We offer both wall mounted and benchtop shelving for reagents, typically in either 18mm MFMDF or 16mm Trespa Toplab Base. Wall shelving is mounted on a bracket system, while benchtop shelving is typically supported by fabricated steel frame.

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From ducted to portable ductless Fume Cupboards, our specialist and experienced partners are at hand to advise and install the right solution.

We provide Fume Cupboards manufactured and installed to meet the industry requirements (e.g. BS EN 14175) in various sizes (External Width 1000mm - 1200mm - 1500mm - 1800mm - 2000mm), Specifications and types (Bench Mounted, Walk In, Double Fronted, Integral Scrubber, HF Type, Thin Wall Bench Mounted) to meet your requirements and safe extraction.

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If you prefer fixed, robust benching or modular benching that offers flexibility and reconfiguration, our laboratory furniture manufacturers can deliver the perfect solution.

Whether you need Class I, II or III to handle Hazard Group 1 to 4 pathogens we can recommend suitable furniture suppliers.

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If you have any specific needs such as Cold Room or Clean Room installation services, Industrial Gases, Liquid Nitrogen, Non-ionising Radiation (LASER), Plumbing, Temperature & Humidity Control or other, we can help.

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