RNA and Peptide Therapies

Confidently meet the specific needs and tight timelines for your RNA or peptide sterile manufacturing with Symbiosis as your trusted partner.

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Nucleic acid therapeutics can achieve long-lasting or even curative effects via gene inhibition, addition, replacement or editing. Breakthroughs in lipid formulation and GalNAc conjugation of modified oligonucleotides have paved the way to efficient delivery. Probably the most important breakthrough in the successful launch of two RNAi therapeutics concerns delivery using LNPs or conjugation chemistry for receptor-mediated uptake and tissue-specific targeting.

Symbiosis has experience of formulation and/or fill-finish of products of a number of these formulation approaches including protein/antibody conjugates, lipid conjugates, nanoparticles, and viral vectors.

Capabilities

Dedicated facility for development and cGMP manufacturing of your RNA and Peptide Therapies, including L-RNA Oligonucleotides, conjugated SiRNA, GalNAc modified RNA Oligonucleotides and SiRNA oligonucleotides. We are experts in small-scale commercial RNA/Oligonucleotide manufacturing.

Bulk Volume

>150 mL ≤50L

Batch Size

≤3000 vial

Services

Development Studies

Validations

Non-clinical / Engineering Batches

Clinical GMP Batches

PPQ & small scale Commercial Batches

Regulatory and Commercial Support

RNA/Oligonucleotide Manufacturing Experience

Pegylated L-RNA Oligonucleotides

Cholesterol conjugated SiRNA

GalNAc modified RNA Oligonucleotide

SiRNA oligonucleotide

Download our RNA and Oligonucleotide Manufacturing Capabilities Sheet

Find out about our RNA and Oligonucleotide manufacturing capabilities and experience by downloading this information sheet.

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Why Symbiosis

Symbiosis are the leading fast access CDMO for clinical or small scale commercial manufacture and our offering is built upon the following principles

Availability

Waiting 6 or even 12 months for a filling slot can be detrimental. We work to your schedule and strive to have availability in as little as 8 weeks.

Schedule

Delivering your product to the clinic on time is essential, given patients are often waiting. Therefore, we execute over 90% of projects within the agreed timeframe.

Speed

We understand the need for results is a critical factor in the progression of clinical trials. Our typical fill-finish campaign takes 12 weeks.

Experience and Expertise

Our dedicated team has handled >600 filling campaigns for mAbs to more challenging ATMPs for >100 customers. You are in safe hands.

Communication

Our service is underpinned by our expert project management team who will keep you informed every step of the way.

Flexibility

Drug development and manufacturing occurs in a dynamic environment. We work flexibly, where possible, to accommodate any changes that you may require.

More RNA and Peptide Therapies information

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