Strategikon Pharma United States

Strategikon Pharma is the developer of Clinical Maestro™, which is an end-to-end elegant cloud-based platform to more efficiently budget, source and manage complex clinical programs. We believe that intuitive technology, complete transparency and effective communication between biopharmaceutical companies and providers will revolutionize the productivity of clinical research.

Clinical Maestro™: Modernize the outsourcing
Company Size (Fulltime employees)
Year of foundation
2016
Please specify your partnering goal
Build awareness of Clinical Maestro value
Headquartner in China
Biotech/Pharma Asset Stage
Medtech Development Stage
Mengdie Peng
Business Development Manager 
Functionality

Trove Therapeutics, Inc. United States

Trove is a semi-virtual biotech start-up located in Rockville, Maryland, USA, developing an advanced biologic asset and seeking funding and partners to conduct clinical trials in respiratory disease. We have data and drug supply on our lead, clinical-stage biologic asset to support up to 3 clinical trials in different respiratory conditions (2 x Phase 1b/2a in COVID and lung transplant; and 1 x Phase 2 in chronic sinusitis). Our biologic, called Therabron, is a replacement for a normally abundant native protein that is deficient in our targeted indications. Replacement therapies have a high approval rate with FDA (>70%) and patients with genetic deficiencies can be selected in some trials to increase our chances of demonstrating efficacy. Therabron was safe in 3 early studies. At present, the quickest path to an approval is likely an Emergency Use Authorization in severe COVID-19 patients, so we're looking for an initial $2M seed/Series A round to fund a Phase 1b/2a clinical trial then need another $16M to produce more drug and perform a convincing Phase 2 trial. We are already talking to several potential corporate partners, have signed one CDA with a top 5 pharma, and a relatively small amount of investment in clinical proof of concept demonstrations will attract at least one partner. Once clinical POC is established in targeted indications, we plan to exit via sale/acquisition or out-license. Our markets are large (3 products x >$1B each US) and deal comps in the respiratory space are $250M each and up. We can maximize our ROI by out-licensing the first indication and re-investing upfront license payment proceeds to advance the drug in further indications, depending on what happens in each field/indication and what we (management team and investors) decide to do.
Company Size (Fulltime employees)
Year of foundation
2018
Stock Market and Ticker/Symbol/Number
private
Please specify your partnering goal
We seek a partner that will license or acquire our lead product, a clinical stage biologic, after a Phase 2 trial. We have a data package and sufficient drug to perform up to 3 clinical trials as described above. Ideally, the partner will have expertise in developing drugs for respiratory diseases.
Funding Status
Pre-seed
Now raising (In USD)
$2M seed round to fund a Ph1b/2a trial, then a $16M Series A round after Ph1b/2a trial completed to fund a Phase 2 trial.
Headquartner in China
Plan in China
To find a licensing partner that has the resources and expertise in respiratory drug development and biologics to advance our clinical-stage candidate, called Therabron, through clinical trials in one or more respiratory indications in China. We prefer to co-develop Therabron in the US and have a good working relationship with our Chinese partner to avoid unnecessary duplication of work.
Assets Information 1: Name|Description|Indications|Stage|IP countries
Therabron (rhCC10 protein)|recombinant human protein - biologic|multiple respiratory|Ph1 & Ph2|none
Biotech/Pharma Asset Stage
Aprile Pilon
CEO 
Functionality