Corporate Update

To Our Shareholders, Employees & Partners:
Our revenue momentum continues as Cumberland has now enjoyed double digit revenue growth for the
fourth consecutive quarter. Revenues totaled $8.7 million in the second quarter of 2017 an increase of 17%
over the prior year period. Ethyol®, our newest brand, contributed $2.1 million in sales during the quarter and
$5.8 so far, this year. Meanwhile, our financial position remained strong with approximately $90 million in
total assets, including nearly $50 million in cash and marketable securities.
One of our key strategic objectives is to maximize the potential of our existing brands - as we believe that an
FDA approved product is a very valuable asset. Towards that goal, we announced in April a new Kristalose®
co-promotion partnership with Poly Pharmaceuticals. Poly's sales organization is featuring our brand with
physician audiences that we don’t cover promoting the benefits of Kristalose to thousands of new medical
providers. We are excited to have secured this partnership and expect Poly’s efforts will support the growth in
Kristalose sales during the multi-year agreement term.
Earlier this year, we announced the acquisition of the exclusive U.S. rights to Totect® through an agreement with
the Clinigen Group plc. Totect is our second oncology support product and complements our current hospital
product line. It’s is an FDA-approved emergency oncology intervention which is indicated to treat the toxic
effects of anthracycline chemotherapy in case of extravasation (drug leakage). With the agreement in place, we
began preparation for the product’s launch and recently, we initiated distribution and sales of Totect in the
United States. We next plan to launch promotion of this important oncology product in September, following
our national sales meeting and brand training. With the introduction of Totect, Cumberland’s commercial
product line now includes seven FDA approved brands.
Meanwhile, we also continued to advance our clinical pipeline programs with initial patient enrollment
underway in our Vasculan® and PortabanTM Phase II studies. We also submitted and obtained FDA clearance for
an investigational new drug (IND) for the BoxabanTM program this year and have now begun initiating its second
Phase II trial at medical centers across the country.
During the second quarter, our earnings were impacted by an allowance for increased Medicaid rebates and a
non-cash adjustment to our tax asset. We do continue to have $44 million in tax loss carry forward available
associated with the prior exercise of stock options. We believe Cumberland’s shares are undervalued and have
continued our share repurchased program.
We recently moved our line of credit to Pinnacle Bank, which is also headquartered in Nashville and one of the
50 largest financial institutions in the United States. The new facility provides for up to $20 million to support
our initiative to acquire rights to select additional products.
Finally, I would like to acknowledge and thank our team for their efforts during the first half of 2017. We all
remain focused on our mission of advancing patient care through the delivery of high-quality pharmaceutical
products. We will be sure to keep you updated on our progress as we work towards a strong finish to the year.


With best wishes,
A.J. Kazimi
Chief Executive Officer
August 2017