Good day, ladies and gentlemen and welcome to the pSivida Fourth Quarter 2016 Earnings Conference Call. At this time, all participants are in a listen-only mode. Later, we will conduct a question-and-answer session and instructions will follow at that time. [Operator Instructions] As a reminder, this conference call is being recorded. I would now like to introduce your host for today's conference Ms. Lori Freedman. Ma'am, you may begin.

Right. Thank you, Kylee. Good afternoon, everyone and thank you for joining us. Earlier this afternoon we released our financial results for the fourth quarter of full year fiscal 2016, a copy of this release is available in the Investors section of our Web site at www.psivida.com. On the call with me today are Dr. Paul Ashton, President and Chief Executive Officer and Len Ross, Vice President, Finance. Before I hand the call over to Paul, I need to remind everyone that some of our prepared remarks are, and answers to your questions maybe, forward-looking in nature. Forward-looking statements are inherently subject to risks and uncertainties. All statements other than statements of historical facts are forward-looking statements and we cannot guarantee that the results and other expectations expressed, anticipated or implied would be realized. Actual results could differ materially from those anticipated, estimated or projected in the forward-looking statements. For a more detailed discussion of risk factors that could impact our future results and financial condition, I refer you to our filings with the SEC, including our Annual Report on Form 10-K for the year ended June 30, 2015. We undertake no obligation to update any forward-looking statements in order to reflect events or circumstances that may arise after this conference call. With that, I’d like to turn the call over to Paul.

Great. Thank you, Lori and welcome everyone to our discussion of our fiscal 2016 full year and fourth quarter results and company update. In fiscal 2016, we made substantial progress in moving forward our products, development agenda, capped by a significant progress in the fourth quarter. Highlights of the quarter included 12-month follow-up that maintains the favorable results for our first Phase 3 trial for Medidur in posterior segment uveitis, and opening an IND for an investigator-sponsored study of a Durasert implant for severe knee osteoarthritis. Those results from pre-clinical testing that has allowed to identify our product candidates to treat wet age-related macular degeneration as an implant delivering a tyrosine-kinase inhibitor. We also have favorable Tethadur pre-clinical results, and a strengthened research and development program. So let’s move on to the details. We have continued to successfully move through the steps toward approval of Medidur for posterior segment uveitis, our lead development product. Following the very favorable top-line results reported in the primary endpoints for our first Phase 3 clinical trial of six months. Our 12 month follow-up, we posted consistent favorable results. Specifically at 12 months, we maintained the same high level of statistical significance in preventing recurrence of disease that was achieved in meeting the primary efficacy endpoints at six months. This is very encouraging. That just over a quarter of the Medidur treated eyes had the recurrence of the disease through 12 months compared to about 85% of control eyes is clearly very impressive. Safety data also remains favorable through the last follow-up visit, which range between 12 and 30 months. The incremental risk of elevated intraocular pressure or IOP in Medidur-treated eyes compared to control was small. And risk was actually lower through the last follow-up than it was through six months. Generally elevated IOP…

Thank you, Paul and good afternoon everyone. I will briefly review our fourth quarter and FY16 results reported earlier today, starting with our financial position. As Paul noted, at June 30, 2016, we had cash, cash equivalents and marketable securities of $29 million, a slight increase compared to $28.5 million at June 30 of last year. During FY16, cash used from operations of $16.3 million was substantially offset by $17 million of cash provided by financing activities, primarily the January 2016 underwritten public offering of our common shares. Our net cash usage was $4.3 million for the fourth quarter of 2016, the same as the prior quarter. We expect that net cash usage will approximate $6.5 million in the first quarter of FY17, primarily due to FY16 incentive compensation payments paid in the quarter, higher CRO payments, and the previously-announced costs of the UK consolidation. We currently expect net operating cash usage in the subsequent quarters of FY17 to average in the range of $5 million to $5.5 million per quarter. On that basis, we anticipate that capital resources at June 30, 2016, and expected cash inflows under existing collaboration agreements, will enable us to fund our current and planned operations into the second quarter of FY18. This estimate includes costs of our ongoing Medidur clinical and regulatory program, but excludes any potential receipts from the commercialization of Iluvien under the Alimera collaboration agreement. Turning now to our full-year FY16 results, revenues decreased by $24.9 million to $1.6 million for the year ended June 30, 2016, compared to $26.6 million for the same period last year. This decrease reflected the $25 million Iluvien FDA milestone that was earned in the first quarter of FY15. Retisert royalty income was slightly more than $1.2 million in FY16, an increase of $68,000, or…

Great, thanks, Len. In conclusion, FY16 was a good year for pSivida. First, we moved forward toward applications for marketing approval of Medidur for posterior segment uveitis. The excellent safety and efficacy results from our first Phase 3 trial for Medidur were maintained through 12 months of follow-up. We're preparing our MAA under the EU centralized procedure, and plan to file in the first quarter of next year. We expect to complete enrollment of our second Medidur Phase 3 trial next month and file for an NDA in the third quarter of calendar 2017. Second, the IND for the investigator-sponsored study of an implant for knee osteoarthritis was opened. Third, we're proceeding with IND-enabling preclinical studies of a bio-erodable TKI insert for wet AMD, and we are continuing pre-clinical research on our Tethadur technology system for both opthalmic and systemic applications. Fourth, we ended the fiscal year with a solid cash position. We are now happy to take your questions. Operator, would you please initiate the Q&A portion of the call?

[Operator Instructions] Our first question comes from the line of Suraj Kalia with Northland Securities. Your line is open.

So, Paul a few questions and I know you are careful not to give too many details but I got a bad habit still try. On the osteoarthritis trial on the IND any sample size what specifically are you targeting follow up period, any color you could provide at this stage?

Yes, it's being run, it's an investigator sponsored study being run in New York at the hospital for special surgery, and this is an initial study, so it's just going to look at six patients for the six month primary end point, which will just be discomfort – this really is aimed at controlling pain rather than disease modification.

Yes, the disease modification I don't, I absolutely understand, so it is just looking at the delta pre and post six months after implantation, is that the right way there is no -- this is just sort of an initial feasibility analysis?

Yes, essentially, it's primarily a safety study.

Fair enough. In terms of the Medidur EU MAA delay Paul, was that a specific data that the EU authorities asked and what kind of data crunching is needed that is causing this delay and is there a chance you all could move the wheels and pull it up again to Q4?

No, there's no chance of being able to bring it forward, it's just the time it takes to crunch the data that we've generated. This isn't a result of any new requirement from the Europeans, it's just -- there was apparently an error made in some of the initial data crunching which didn't alter the top line data at all, but it caused us to have to get the CLOs to re-run some of the analyses which has just delayed everything.

And that error was clocked by the EU authorities, or you guys discovered it?

No, no, no, it was caught by us, we haven't submitted anything to the EU authorities.

Okay. But the P values and percent recurrence and IOP, all those on -- in the intent to treat or nothing has changed as a result of this error?

That's correct. It's just one minor error that makes you -- requires you to go back and check everything else, and everything else is fine.

Paul, Alimera put up a pretty decent quarter for their numbers reported. What other royalties on ILUVIEN are there, if I remember correctly, they had like $9.8 million or $10 million run rate, have you all not -- it seems like you’ll have not crossed the minimum threshold yet, over your 20% of net profits, royalties start kicking in?

Yes that hasn't been quite for us yet, it hasn't -- it kind of -- it’s lumpy in some quarters, the payment is due another is not, but we're obviously optimistic that sales will continue to improve and we'll start to see checks on a more regularly basis.

And finally Paul on Medidur, any color you’ll could provide on your discussions with strategics, partners in terms of distribution once it gets approved? Thank you for taking my questions.

We're certainly having some of those discussions, and until they reach a conclusion, they are only discussions.

Thank you. And our next question comes from the line of Vernon Bernardino with FB&R. Your line is open.

When do you expect when we'll know what the TKI that is being used for the wet AMD indication will be revealed?

So nothing to be gained by revealing it at the moment, so I don't know that we need to reveal it, it's a physical small molecule, it's on the market, it's a cancer drug, one known mode of action inhibits VEGF and PDGF, not sure what else we need to fill in there.

Okay. And you had mentioned that you've implemented the first of two IND enabling studies, can you tell what those IND enabling studies are, what is the second one being pursued?

So, for the IND, you need a non-GLP tox PK study and two GLP tox studies. So we have started the first of those and we are doing the second. Second one should, animals should be dosed within about two weeks I think.

Okay. And it sounds very simple then. When do you think that we will see results?

Tox studies again, it would take longer than you hope, because of the final report. But these are four-month Tox studies.

They are 12-months studies?

Four months.

Four months, okay. Four-month studies okay.

We hope to be able to file an IND within a year in the current fiscal year.

Okay. And then switching to Medidur, can you compare, what are you seeing and can you compare the patient enrollment seen in the second Medidur Phase 3, versus the first Phase 3. Are there any difference in enrollment observed?

This is the first and the second Phase 3. The second Phase 3 is designed as 150 patient study and we expected it to be all done next month.

Okay. Last question for me and I’ll get back in the queue. So it says the new drug application based on both Phase 3 trials is planned for the third quarter of 2017, and just want to confirm that is calendar year or fiscal year?

Calendar year.

[Operator Instructions] Our next question comes from the line of Matt Kaplan with Ladenburg. Your line is open.

A couple questions, wanted to, can you give us a little bit of detail in terms of the new injector, the new device, the new inserter that you have developed? And how it differentiates from the prior inserter, and you mentioned some positive data that you announced recently, I guess, last month, in terms of the user usability study. Can you give us a sense of that as well?

Yes certainly. So oddly enough, injecting things into eyes is actually quite difficult. There has been a variety of different-size inserters developed and approved. I think the biggest one is probably the Allergan's Ozurdex inserter, which is, I think a 22 gauge I believe, which is big. You have to carefully introduce it in the eye to avoid leaving a hole that would allow the vitreous to prolapse out of. Then there is the 25 gauge, which is the one that we developed and used with Iluvien, which is smaller, but it's still not perfect. You have to push the thing pretty hard to get it in. Now the 27 gauge, we actually use a size needle to make the hole that is the same size and type of needle that is occasionally used for injections of suspensions of Triamcinolone Acetonide, so it's size that is much more normally used by physicians. It's a simpler procedure. It's easier to get in. And it's interesting that with all the technology that's out there, that one of the -- technically one of the hardest things is to develop and design a dumb needle that is easy to get into an eye, but that is the way it is.

Okay. And what's your IP around the inserter?

Patents have been filed and I believe we have got of nests of patents covering it, and some are being issued and some are about to issue.

And then in terms of Tethadur, you mentioned some positive pre-clinical data with Avastin that you developed. Can you give us a sense of the timeline going forward to that program, and some milestones as well?

Sorry what is that, for which program please?

For the Tethadur the Avastin I guess you had, yes.

So we're talking to a couple of potential partners for that program. We are interested in partnering that and moving it forward with systemic administration of antibodies, which is perhaps the biggest opportunity, when you think about it. So this technology, for folks who may not be familiar, enables the sustained delivery of big molecules, like antibodies. The antibody marketplace right now is huge. With a lot of these molecules coming off patent, it's creating this enormous biosimilar industry. And if you follow the space, you will see lots of patents being filed and defenses, and all kinds of legal issues around things like Humira, and Remicade, and all these things, which are administered as performing normally, and the problem that you have for the biologics is that unlike small molecules, where there is a well-established lifecycle management and strategies you can have, tablets that go blue, tablets that say it's this thing, there's really nothing like that at all for the biologics. And the Tethadur technology is designed to provide sustained release, so for instance, so you could go from an injection of Humira once every two weeks to an injection every month or every two months or in the eyes an injection of Eylea or Lucentis every month, to an injection every three months, and every six months, and every year. So that's the plan there, and we're optimistic we will be able to move that technology forward. It's probably best done in conjunction with a much larger plan. Again, if you take the example of Humira, we have a technology that would potentially deliver that molecule. That would best be done in collaboration with AbbVie, because I don't think a Company our size can realistically believe they can take on AbbVie. So that was a very long-winded explanation. I hope I answered your question.

Thank you. And I am showing no further questions at this time. I'd like to turn the call back to Dr. Ashton for closing remarks.

Great, thank you. I'd like to thank you all for joining us today and I look forward to speaking with you again in the next quarter. In the meantime of course if you have any additional questions please feel free to contact us. Thank you.

Ladies and gentlemen thank you for participating in today's conference. This does conclude the program and you may all disconnect. Everyone have a wonderful day.