Velan Calls for Increased Transparency at Progenics Pharmaceuticals During Q1 Earnings Call

ALPHARETTA, Ga., May 8, 2019 /PRNewswire/ -- Velan Capital, L.P. (together with its affiliates, "Velan" or "we"), one of the largest stockholders of Progenics Pharmaceuticals, Inc. ("Progenics", "you" or the "Company")(NASDAQ: PGNX), today publicly called on the Company's management team and Board of Directors (the "Board") to increase the level of disclosure and transparency when Progenics reports first quarter results on May 9, 2019. Velan also announced that it filed a preliminary proxy statement and accompanying GREEN proxy card yesterday seeking stockholder support against the election of Peter J. Crowley and Michael D. Kishbauch at the Company's 2019 Annual Meeting of Stockholders (the "Annual Meeting") to send a clear message that the status quo is no longer tenable and that meaningful change is required.

Velan believes that Progenics has long exhibited substandard disclosures on key matters, which become more vital as time and resources are squandered. Most recently, Mark Baker, Progenics' Chief Executive Officer, refused to take time for investor questions after his presentation at the Needham Healthcare Conference in April 2019. Progenics stockholders deserve more, especially as the Board and senior management continue to underperform - which is why we are seeking stockholder support to hold certain members of the Board accountable at this year's Annual Meeting.

Velan has issued a series of questions that it believes should be answered by Progenics:

AZEDRA


     1. Patient & Hospital/Facility Access. If AZEDRA
          was "commercialization ready" per the Company's
          2017 corporate goals as determined by the Board,
          why has it taken more than eight months from
          approval for a patient to be dosed? What did you
          tell hospitals and physicians while patients
          have waited for this product? How many eligible
          patients have you identified through the centers
          your sales representatives have engaged? Given
          the small number of high-volume use hospitals,
          how many P&T committees have you interacted with
          which now have approval/drug acceptance? Have
          any P&T committees chosen MIBG over AZEDRA or
          rejected AZEDRA? What are hospital/facility
          economics for those that choose AZEDRA vs. MIBG?
          Have you or will you take action to remove
          compounded MIBG from the market?




     2. Payors. Have any payors approved AZEDRA? How many
          payor plans have already completed a benefits
          check as a result of a patient being scheduled?
          Have any payors outright rejected AZEDRA?




     3. Manufacturing. At what time was the product
          commercially available from a manufacturing
          standpoint? Was it available after Progenics'
          February 2019 facility acquisition or after its
          April 2019 agreement with International
          Isotopes? Which facility has supplied commercial
          product (if any) to date? Why did Progenics need
          this agreement given that you noted its facility
          is adequate in the Company's February 2019 press
          release? Redundancy when a patient hasn't been
          dosed seems excessive unless there is an issue
          you haven't made shareholders aware of.




     4. Expectations. Please provide AZEDRA sales
          expectations for 2019. As investors, how do we
          gauge if AZEDRA is on track relative to
          management's plan? Has AZEDRA's delay impacted
          your perspective on its potential peak sales
          (since patients since July 2018 have likely
          continued to take compounded MIBG removing them
          from the pool of eligible AZEDRA patients for an
          extended period of time)?




     5. Intellectual Property. What IP covers AZEDRA
          beyond its FDA Orphan Drug Exclusivity given
          that nearly one year of this seven-year period
          has passed with no disclosed sales to date? Does
          the Company have a protection plan of which
          stockholders are unaware?




     6. Basket Trial. Have you discussed your approach
          with the FDA? If so, when was the discussion
          held and what was the FDA's feedback?



MIP-1095


              7.               What has been discussed with the
                                 FDA regarding MIP-1095? Has the
                                 Phase 2 trial design been agreed
                                 upon? Did you consider adding a
                                 monotherapy arm in the Phase 2
                                 trial design?



              8.               Is 2026 a reasonable assumption
                                 for MIP-1095's launch per the
                                 Company's disclosure in its 2018
                                 10-K? The 2017 10-K noted 2025
                                 as the expected timing of MIP-
                                 1095's launch - should
                                 investors expect further delays?

Corporate


              9.                What specific performance can the Company
                                  point to that explains the 80% and 100%
                                  performance metrics given by the Board
                                  relating to "maximize[ing] value of AZEDRA"
                                  and "increase[ing] value of pipeline",
                                  respectively, as disclosed in its amended
                                  2018 10-K, given that in 2018 AZEDRA went
                                  five months with no sales, 1404 failed its
                                  clinical trial and 1095 trial had not begun?



              10.               If AZEDRA was "commercialization ready" and
                                  FDA-approved, why is the probability of MIP
                                  commercial milestone payment only 90% per
                                  your 2018 10-K disclosure? Is there another
                                  risk of which stockholders were not made
                                  aware?

Financial


              11.               What is the cost of, and capacity
                                  covered by, the manufacturing
                                  arrangement with International
                                  Isotopes? Why have you not publicly
                                  disclosed this arrangement?



              12.               How much will the MIP-1095 Phase 2
                                  trial and AZEDRA basket trial cost?



              13.               Why has the Company neither
                                  refinanced the Relistor non-
                                  recourse debt nor borrowed further
                                  against this valuable royalty
                                  stream to provide accretion (vs.
                                  management's seeming preference for
                                  dilutive equity issuances)?

Investors and analysts have been asking many of these vital questions but have received little in the way of meaningful answers. Velan believes this lack of transparency, together with the Company's persistent underperformance and concerning corporate governance actions, necessitates immediate change in the composition of the Board. Stockholders deserve more transparency and accountability.

Investor contacts:

Deepak Sarpangal
(415) 677-7050
campaign@velancapital.com

Okapi Partners LLC
Pat McHugh / Jason Alexander
(212) 297-0720
info@okapipartners.com

CERTAIN INFORMATION CONCERNING PARTICIPANTS

Velan Capital, L.P., together with the other participants named herein (collectively, the "Participating Stockholders"), has filed a preliminary proxy statement and accompanying GREEN proxy card with the Securities and Exchange Commission ("SEC") to be used to solicit votes against the election of certain directors of Progenics Pharmaceuticals, Inc., a Delaware corporation (the "Company"), at the Company's 2019 Annual Meeting of Stockholders.

THE PARTICIPATING STOCKHOLDERS ADVISE ALL STOCKHOLDERS OF THE COMPANY TO READ THE PROXY STATEMENT AND OTHER PROXY MATERIALS AS THEY BECOME AVAILABLE BECAUSE THEY WILL CONTAIN IMPORTANT INFORMATION. SUCH PROXY MATERIALS WILL BE AVAILABLE AT NO CHARGE ON THE SEC'S WEB SITE AT HTTP://WWW.SEC.GOV. IN ADDITION, THE PARTICIPANTS IN THIS PROXY SOLICITATION WILL PROVIDE COPIES OF THE PROXY STATEMENT WITHOUT CHARGE, WHEN AVAILABLE, UPON REQUEST.

The participants in the proxy solicitation are Velan Capital, L.P. ("Velan"), Altiva Management Inc. ("Altiva"), Balaji Venkataraman, Virinder Nohria, LTE Partners, LLC ("LTE"), LTE Management, LLC ("LTE Management"), Melkonian Capital Management, LLC ("MCM"), Ryan Melkonian, Terence Cooke and Deepak Sarpangal.

As of the date hereof, Velan directly beneficially owns 6,030,000 shares of common stock of the Company ("Common Stock"). Altiva, as the general partner of Velan, may be deemed the beneficial owner of the 6,030,000 shares of Common Stock owned by Velan. Mr. Venkataraman, as the sole shareholder of Altiva, may be deemed the beneficial owner of the 6,030,000 shares of Common Stock owned by Velan. As of the date hereof, Mr. Nohria directly beneficially owns 110,000 shares of Common Stock. As of the date hereof, LTE directly beneficially owns 1,625,000 shares of Common Stock. MCM, as the sole investment advisor to LTE, may be deemed the beneficial owner of the 1,625,000 shares owned by LTE. LTE Management, as the sole manager of LTE, may be deemed the beneficial owner of the 1,625,000 shares owned by LTE. Mr. Melkonian, in his capacities as (i) the sole manager and majority member of LTE Management and (ii) the Chief Investment Officer, Managing Member and majority owner of MCM, may be deemed the beneficial owner of the 1,625,000 shares owned by LTE. As of the date hereof, neither of Terence Cooke or Deepak Sarpangal own beneficially or of record any securities of the Company.

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SOURCE Velan Capital, L.P.