Good day, ladies and gentlemen. And welcome to the Q4 2014 Geron Earnings Conference Call. My name is Ian, and I'll be your operator for today. At this time all participants are in listen-only mode. We will conduct a question-and-answer session towards the end of the conference. [Operator Instructions] As a reminder, the call is being recorded for replay purposes. I'd like to turn the call over to Mr. Kevin Eng from Investor Relations. Please go ahead, sir.

Thank you, Ian. Good morning, everyone. And thank you for joining us for the Geron fourth quarter and year end 2014 earnings call. With me today are Dr. John Scarlett, our President and Chief Executive Officer; and Olivia Bloom, our Executive Vice President, Finance and Chief Financial Officer; and Melissa Behrs, our Executive Vice President, Business Development and Portfolio and Alliance Management. This afternoon, we issued a press release that reports results for the fourth quarter and year ended December 31, 2014. This release can be found on our website at www.geron.com. Today's call is also being webcast live on our website and we will be -- and will be available for replay until April 3rd. Before we begin, I would like to remind listeners that except for statements of historical fact, the statements during this conference call are forward-looking statements under the Safe Harbor provisions of the Private Securities Litigation Reform Act of 1995. These include, without limitations, statements regarding the timelines, prospects and plans for imetelstat, including clinical study initiation and IND transfers, the therapeutic potential and safety of imetelstat, financial or operational projections or requirements and Geron desire to diversify its product portfolio. These statements involve risks and uncertainties that can cause actual results to differ materially from those in such forward-looking statements. These risks and uncertainties include without limitation that imetelstat is safe and efficacious, enabling Geron to receive continuation, milestone and royalty payment from Janssen, Geron's dependence on Janssen for the development, regulatory approval, manufacture and commercialization of imetelstat, unanticipated challenges in transferring imetelstat INDs and unanticipated expenses and charges not currently contemplated. Additional information and factors that could cause actual results to differ materially from those in the forward-looking statements are contained in Geron's periodic reports filed with the Securities and Exchange Commission under the heading Risk Factors, including Exhibit 99.1 of Geron's current report on Form 8-K filed on November 13, 2014. Undue reliance should not be placed on forward-looking statements, which speak only as of the date they are made, and facts and assumptions underlying those forward-looking statements may change. Except as required by law, Geron disclaims any obligation to update these forward-looking statements to reflect future information, events or circumstances. We will begin today's call with a summary of the fourth quarter and year end operating results from Olivia, and then Chip will comment on recent events and the impact of our business. Olivia?

Thanks, Kevin. Good afternoon. Net loss for the fourth quarter of 2014 was $8.9 million or $0.06 per share, compared to $9.3 million or $0.07 per share for the comparable 2013 period. Net loss for 2014 was $35.7 million or $0.23 per share, compared to $38.4 million or $0.30 per share for 2013. Revenues for the fourth quarter of 2014 were $178,000 compared to $225,000 for the fourth quarter of 2013. Revenues for 2014 were $1.2 million, compared to $1.3 million for 2013. Revenues for the fourth quarter and year ended 2014 and 2013 periods reflect royalties and license fees from various agreements. Total operating expenses for the fourth quarter of 2014 were $9.2 million, compared to $9.5 million for the fourth quarter of 2013. Total operating expenses for 2014 were $37.5 million, compared to $40.2 million for 2013. Operating expenses for the 2013 fourth quarter and 2013 year-to-date periods included restructuring charges of $430,000 and $1.5 million, respectively in connection with the company’s decision to discontinue its discovery research programs and close its research lab facility in 2013. Research and development expenses for the fourth quarter of 2014 were $4.4 million, compared to $5.1 million for the fourth quarter of 2013. Research and development expenses for 2014 were $20.7 million, compared to $23.2 million for 2013. The decrease in research and development expenses for the fourth quarter and year ending December 31, 2014 compared to the same period in 2013, primarily reflects the net result of lower clinical trial expenses with the wind-down of the imetelstat trials in solid tumors and GRN1005 trials in patients with brain met and reduced personnel-related and other research costs resulting from previous restructuring and the discontinuation of the company's discovery research program, all partially offset by higher costs for the manufacturing imetelstat drug…

Thanks, Olivia, and good afternoon everyone. Before I describe our planned business activities in 2015, I’d like to comment on our ongoing collaboration with Janssen for imetelstat. The transition of the operation to the imetelstat program is progressing very well. We've been pleased by the enthusiasm and energy shown by the Janssen team, the level of corporate commitment they’ve shown as well as the highly collaborative interactions that we’ve had with them. We’re in the process of transferring the operational execution of clinical, regulatory and manufacturing activities for imetelstat to Janssen. And we expect the majority of these transition activities to be completed by mid-2015. We anticipate that prior to the initiation of the initial Phase 2 MF Study, imetelstat INDs will be transferred to Janssen. At that time, Janssen will also assume sponsorship for the MF pilot study being conducted at Mayo Clinic by Dr. Tefferi. As a reminder, no new patients are being enrolled in this study and the remaining patients in the study continue to receive imetelstat treatment. Upon transfer of the sponsorship of the MF pilot study to Janssen, Jannsen will assume responsibility for collecting the data and information from the study. We expect Dr. Tefferi will submit an abstract with data from the MDS cohort of patients treated in that study to a medical conference in 2015. Although we anticipate the demands from Janssen on our clinical regulatory and manufacturing and operating teams will decrease significantly in the second half of the year we plan to continue to diligently represent Geron’s interests on the imetelstat joint development committee and joint steering committee as well as on several joint working group's operating under the purview of the joint steering committee. Through these committees, our responsibilities include active review and approval of all clinical studies, manufacturing plans…

[Operator Instructions] This comes from the line of Chad Messer at Needham & Co. Please go ahead, Chad.

Great. Thanks for taking my question. Hi, Chip and everyone. Can you talk a little bit more about the positions that are being eliminated? If you're going after trying to diversify and bring in a new Phase 1 or 2 compound, might you just be getting rid of people that you might need to hire back?

Chad, the majority of the positions that are being eliminated are in the clinical operations and technical operations area, with a few people who provide other support for those individuals. We certainly believe that the remaining core of the employees, including the Senior Management Team can form a pretty solid foundation for the development of a new asset. And I must say, of course if we acquire or in-license an asset, we will probably need to recruit additional personnel. But that’s -- to be honest with you an uncertain timeframe for that and also exactly what will be needed will be determined by that asset. So, we felt that it was very prudent to take these actions today and we will fill in as necessary in the future.

Understood. Thank you.

Thank you for your question. We have another question for you. This one is from the line of Brian Klein at Stifel. Please go ahead, Brian.

All right. Thank you for the updates and for taking my questions. First, I just wanted to get a better sense of the ongoing activities involving business development. Could you give us a sense of where you are in terms of your diligence? Could you give us an update on potential timing where we might see a new product in-license? Are you limiting yourself to just one product or are you potentially willing to in-license a platform or portfolio of products, any additional details would be great? Thank you.

Thanks, Brian. So the process has recently been started and this is obviously a very competitive process. So, I don't think we are going to go into a deep level of detail regarding our search criteria at this time. But I think Melissa might have a few comments about sort of the general commentary around that.

Sure. Obviously, not surprisingly, our thinking right now is that our search will remain focused on oncology and given our expertise in heme malignancies, we will be particularly interested in evaluating opportunities in that space. In terms of stage of development, we are not going to rule out the possibility of finding something attractive at the pre-clinical stage, our focus will rest mostly in the Phase 1 to early Phase 2 area and stage of development. The timing, as I'm sure you can appreciate it is hard to predict how long these processes will take, particularly we are not in any particular rush to bring something in. I think what’s most important is that we find and focus on assets that are of high quality and we will take the time that’s necessary to really find that type of asset.

And then with regard to one versus more, I think, Brian, we have an open mind about that. Obviously, the goal of most people who do these processes is to find a platform technology with a lead candidate that looks really good and we would never turn our nose down at that. But on the other hand, history suggests that that doesn’t happen every time. So it’s not something that is not a criterion that we are applying in any specific way.

Okay. Great. Thanks for the additional details. And then just moving on to the ongoing study with Dr. Tefferi, is it -- are you guys capable of giving an update there in terms of how many patients remain on therapy, and if you -- we can expect potentially to see an update at this year’s ASCO?

As of January the 30th, 20 patients out of the 80 patients that were enrolled in Dr. Tefferi study continue to receive imetelstat treatment, Brian. That includes 15 out of 60 patients with MF, four out of the nine patients with RARS MDS and one out of the nine patients with last Phase MF. With regard to future clinical studies, sorry, future meetings, we don’t have any specificity about where that will be, but I am unaware of anything that has been submitted to ASCO. So it will probably be after ASCO, but we still expect something for this year.

Great. Thank you for taking my questions.

Sure.

Thanks for your question, Brian. We have another question for you. This one is from a line of Thomas Yip at MLV & Co. Please go ahead, Thomas.

Hey, everybody. Thank you so much for taking my questions. I would just have a quick one for Olivia first. Can you please tell us how is the $35 million license fee from Janssen that I assume is already received? How is that accounted for in the P&L?

So you are correct, Thomas. We did receive that money at the end of 2014. So that’s why it’s included in the cash balance sheet. You will see on the balance sheet a large increase in our current liabilities because of the recognition of deferred revenue for that $35 million as of the end of '14. Upon conversations and agreement with our auditors, we’ve determined that we would be recognized the revenue from that upfront payment once the transfer activities related to the program have been complete and we expect that to be occurring sometime around between Q2 and Q3 of this year.

Okay. And will that be the lump sum immediately recognized or will that be amortized over a certain period of time?

It will be recognized in entirety.

Okay. And my next question, I know is a little bit early since we’re just looking at starting MF and MDS trials in 2015. But regarding future plans for AML, I am just wondering what is the scope and the economics of potentially expanding into AML?

Thomas, this is Chip. The agreement with Janssen contemplates two, or specified I should say, two initial studies that are well laid out. The first one is the Phase 2 MF study. The second is the Phase 2 MDS study, both of which we expect to initiate this year. Beyond that although AML as you point out is referred to in the CDP, etcetera there are no specificity around that. And until we gain greater specificity, we really can’t give anything and we really can’t answer your question at the moment. So how that plays out will be talked about a little bit in the future at some point. But as of right know, I really don’t have anything we can tell you about it.

Understood. Thank you so much again for taking my questions.

Thank you. We have another question for you. This one is from George Zavoico at [Jones Trading] [ph]. Please go ahead, George.

Thank you. Hi, Chip, Olivia, Melissa and Kevin. Thank you for taking my questions. It seems to me that pretty much the whole imetelstat package is moving over to Janssen. And without -- and with you having discontinued your research -- or sorry discovery programs, what about learning more about telomerase by chemistry and physiology in these diseases, biomarkers that sort of thing? There is still a lot that can be learned as all of that then moving to Janssen as well, especially with regard to post the malignancies because telomerase is present in all cancers?

Yes. That’s a great question, George. Thank you. The answer is yes, it is moving over to Janssen. I am happy to say they have an awful lot of people in their translational program and they have been -- even though we haven’t spoken in any specificity around it, I can assure you that they are very interested in this. And when we have something to report, we will. But I feel very confident that these areas are going to continue, generally speaking, translational research, especially into the mechanism of action of the drug and deeper into telomerase actions in various diseases and so forth. I think we will see programs being put together. It’s too early to make any promises in that regard or to have any specifics, but that is going to go over to Janssen.

The partnership however just includes heme malignancies. So if that happens, does Geron get any economics from that if it happens?

Yes. So actually the partnership covers all human therapeutics uses George, including non-heme malignancies and even should there be any other uses. So they’ve licensed the product for all human therapeutics uses. So obviously, the scope of interest is broader than just heme malignancies at some point.

Yes. There was a minor point I recall when the agreement was first announced. Well, good luck with that. I hope the platform emerges over the course of the next few years and moves beyond the heme malignances. Good luck. And thank you. Look forward to start with the trials and data come out later this year. Thank you.

Thank you. Thank you very much, George.

Thank you, George. We have a further question for you. This one is from Charles Duncan of Piper Jaffray. Please go ahead, Charles.

Hi, guys. Hi, Chip. Hi, Olivia. Thanks for taking my question. And I apologize if you addressed this earlier in your prepared remarks or answers to other questions I hop timely. But I wondered if you could provide us any color on you’re evaluating other technologies or potential assets? Is that something that is an ongoing set of efforts? Or are you focused more on working with the current partnership?

It’s definitely outside of our BD process. It’s definitely outside of the current Janssen collaboration, which is really focused very much on imetelstat. The process has really just recently begun. This is -- I commented earlier, this is a very competitive process. So we're not going into a deep level of detail regarding our search criteria at the time. But fundamentally, we’ve commented that we are focusing predominantly, and although we will not rule out a preclinical opportunities primarily looking at Phase 1 and early Phase 2 compounds. And while we remain opportunistic for other general oncology related assets, we certainly will be particularly focused on heme malignancies, which is the therapeutic area that we know particularly well.

Yes. That makes sense to me, Chip, and without giving guidance or setting expectations, but could you foresee that process coming to fruition over the course of the next 12 months?

Well, I think that if you look historically at these processes in our industry and sort of look at them from when you start to win, you come to some sort of conclusion, 12 months is pretty good length of time. But as you say, we’re certainly not in a position to be promising or even leading anyone on with regard to any specificity, because we’re still early in the process. And so it's a little tough to do so.

Okay. That makes sense to me. Thanks for taking the questions.

Sure.

Thank you, Charles. That ends the questions for today. So I’d now like to turn back to Chip for closing remarks.

Well, thanks everybody for your time today. We look forward to future discussions about the activities of the company and about imetelstat progress with Janssen and also with regard to our own other non-imetelstat related activities. Thanks a lot. And have a good day.