When specialists join forces to better serve HMNC Brain Health
in its phase II clinical trial
HMNC Brain Health is a disruptive clinical stage biopharmaceutical company pioneering Precision Psychiatry, powered by its AI Platform, and focusing on Treatment-Resistant Depression (TRD) and Major Depressive Disorder (MDD).
Nelivabon program is one of HMNC Brain Health’s flagship precision psychiatry programs for MDD, in which the company develops the drug candidate Nelivaptan (BH-200) together with a companion diagnostic test. The investigational medicinal product (IMP), BH-200, is a vasopressin 1b receptor antagonist.
Started in May 2023, the clinical trial is a 14-weeks, multicentre, double-blind, randomised, placebo-controlled phase II study with an 8-weeks treatment period to assess the efficacy and tolerability of a fixed dose of BH-200 (250 mg BID) in outpatients with MDD. HMNC Brain Health expects 324 patients to be included in this clinical trial.
HMNC Brain Health
« Our strategic alliance with DELPHARM & CREAPHARM has enabled us to take forward our compound to a Phase II clinical study as per the planned timelines. We look forward to continuing our successful collaboration for our next projects as well. »
DELPHARM Development and CREAPHARM CLINICAL SUPPLIES have collaborated to fully meet HMNC Brain Health’s need and makes its task easier while handling end-to-end operations for both non-GMP technical batches and clinical batches:
Development Project Manager
« Hand in hand collaboration and team spirit between each partner leads to a successful project: making clinical batches available in a record time for patients. »
CREAPHARM CLINICAL SUPPLIES
« Each specialist contributed to the success of this clinical trial set-up, sharing expertise & experience, with an innovative approach aimed at moving things forward. »
Due to limited API availability, Delpharm was able to reposition manufacturing batches size and reached a successful dissolution profile.
The teams adapted the manufacturing planning in order to handle the technical batches manufacturing with conform and robust process and results in a short timing, due to the API’s synthesizing requirements and specifications. DELPHARM Development team was able to adapt the capsule quantity of each dosage according to the clinical trial design which evolved during the project.
Effective blinding includes all the related traits of the drug AND of its packaging.
To ensure BH-200 50 mg, BH-200 100 mg and placebo caps likelihood, size 0, Swedish-orange hard gelatine capsule are used for manufacturing of dosage strengths 50 mg and 100 mg and matching placebo (without nelivaptan dose).
The primary and secondary packaging steps are fitted to the maximum quantity available of each dosage and placebo at time.
The QC check ensures the likelihood as a mandatory prerequisite.
250 shipments are planed, from CREAPHARM CLINICAL SUPPLIES Le Haillan to the clinical sites in 7 European countries.
To meet local regulations, CREAPHARM’s depot partner in Serbia acts as the importer and broker for clincial distribution to this country.
Every treatment unit is labelled in the 11 languages requested to address the target countries in the clinical trial. Booklet labels were designed by CREAPHARM Project Management Team. The variable data are printed in-house for more flexibility.
patients do not respond sufficiently to their 1st antidepressant medication
SOURCE: FINAL PROTOCOL OF THE BH-200-03
DELPHARM DEVELOPMENT is the business unit of DELPHARM offering full development services for a large range of dosage forms for new chemical entities or innovative fixed dose combinations there of clinical batches supply for Phase 1-3 for OSD and injectable dosage forms. DELPHARM is a worldwide leader in contract development and manufacturing (CDMO) of medicines for pharmaceutical companies.
Customer Satisfaction, Excellence, Agility and Co-Sucess are CREAPHARM’s core values.
It’s because DELPHARM DEVELOPMENT is in line with our approach that we set up a strong partnership. Our respective teams easily work together to offer a comprehensive and efficient service offer to our common customers.
FIRST PATIENT IN – Accelerating the clinical trial start and make research progress
METHOD TRANSFER – Production method
PARTNERING WITH JOB SPECIALISTS
Leading different vendors and related operations
QP-RELEASE – Entrusting therelease to a certifying site
DEADLINE COMMITMENT – To meet the First Patient In objective
MANUFACTURING – Method testing, transfer and then scale-up
LIKELIHOOD – Verum and Placebo manufactured by the same team. Adapted packaging item purchase and blistering/walleting runs
AGILITY – Rescheduling
EXPERIENCE & ADVICE – Providing the best option for customer & patients
Working hand in hand with customers and partner vendors with trust
ADAPTED EQUIPMENT – Smallbatches
SCALE-UP – Method/Process transfer
WALLET CARDS redesigned to servecost optimization
BOOKLET LABELS – To manage 11 languages, avoid IMP waste (no unit allocation) & limit labelling operations
Quality/Regulatory expert advice, QP-release & shelf-life extension
CSR positive impact – Reliable AND reusable insulated boxes for distribution