Coriolis Pharma offers Biophysical characterization, formulation and stability of biologics. Services should be matched to the intended study and assay requirements.
KKR Health Care Strategic Growth Fund II投资，轮次名称及金额未披露。
Profile review: 2026-11-05 · Fields retain their individual source dates. Undisclosed values are not zero; early or historical events do not establish the latest financing. Awards and acquisitions are distinguished from equity rounds.
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Technology, programs & evidence
A CRO specializing in biologic drug products, offering early- through late-stage formulation and analytical development for high-concentration, liquid, and lyophilized products; U.S. laboratory operations were publicly disclosed in 2026.
Biophysical characterization, formulation and stability of biologics
Specialist contract research/testing services
Program / service
Target / indication
Representative stage
Evidence & scope
Formulation development / contract manufacturing capabilities
Defined by the client project · Defined by the client project
Services / platform
Service pages do not establish human evidence for every project
Related news & literature
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A Communications Chemistry study reports RaPiD-mAb-MS, combining plate-based preparation with direct-infusion mass spectrometry for antibody peptide mapping. The original abstract describes analysis of 96 samples in about 1.5–2 hours, routinely exceeding 95% sequence coverage, across 28 antibodies and more than 2,000 samples. The reported comparisons cover several modifications and sequence variants; broader method suitability still requires evaluation.
A Nature Communications study reports a peptide–oligonucleotide nanohybrid for bone-targeted miR-26a-5p delivery. The original abstract describes reduced GSK-3β expression and stabilization of HIF-1α, supporting coupled bone formation and angiogenesis. Systemic administration limited skeletal and vascular injury in a rat glucocorticoid-induced bone-loss model. This is preclinical miRNA delivery, not oral cyclic peptide therapy or human efficacy evidence.
FDA granted accelerated approval to amivantamab and hyaluronidase-lpuj for adults with recurrent or metastatic head and neck squamous cell carcinoma after platinum chemotherapy and an anti-PD-(L)1 antibody. HPV-associated oropharyngeal cancer is excluded. In the 102-patient OrigAMI-4 efficacy population, response rate was 42%. Continued approval requires confirmatory clinical benefit; this is not traditional full approval.
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Company service pages support the stated scope but do not establish clinical validation of every dosage form or client program.
Service-provider record; no proprietary drug pipeline implied. Confirm laboratory qualification and project suitability.
