Y-mAbs to Announce 2019 Financial and Operating Results on March 12, 2020

On March 5, 2020 Y-mAbs Therapeutics, Inc. (the "Company" or "Y-mAbs") (Nasdaq: YMAB) reported that it will report its 2019 financial and operating results on Thursday, March 12, 2020, after the close of the U.S. financial markets (Press release, Y-mAbs Therapeutics, MAR 5, 2020, View Source [SID1234555233]). The announcement will be followed by a conference call and webcast with the investment community at 4:30 p.m. ET. Participating on the call from Y-mAbs will be Thomas Gad, Founder, Chairman and President; Dr. Claus Moller, Chief Executive Officer; and Bo Kruse, Chief Financial Officer.

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Conference call and webcast details:

Investors (domestic): 877-407-0792
Investors (international): 201-689-8263
Conference ID: 13699294

To access a live webcast of the update, please use the following link:
View Source

Savara to Report Fourth Quarter/Year-End 2019 Financial Results and Provide Business Update

On March 5, 2020 Savara Inc. (NASDAQ: SVRA), an orphan lung disease company, reported that the Company will report fourth quarter/year-end 2019 financial results and provide a business update on Thursday, March 12, 2020. Savara management will host a conference call/webcast at 4:30 p.m. Eastern Time (ET)/1:30 p.m. Pacific Time (PT) (Press release, Savara, MAR 5, 2020, View Source [SID1234555232]).

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Shareholders and other interested parties may access the call by dialing (855) 239-3120 from the U.S., (855) 669-9657 from Canada, and (412) 542-4127 from elsewhere outside the U.S. and requesting the "Savara Inc." call. A live webcast of the call can be accessed on the Investors page of Savara’s website at View Source

Approximately one hour after the call, a telephone replay will be available and will remain available through March 19, 2020 by dialing (877) 344-7529 from the U.S., (855) 669-9658 from Canada and (412) 317-0088 from elsewhere outside the U.S. and entering the replay access code 10139201. A webcast replay will be available on the Investors page of Savara’s website and will remain available for 30 days.

HARPOON THERAPEUTICS TO REPORT FOURTH QUARTER 2019 FINANCIAL RESULTS AND PROVIDE CORPORATE UPDATE

On March 5, 2020 Harpoon Therapeutics, Inc. (Nasdaq: HARP), a clinical-stage immunotherapy company developing a novel class of T cell engagers, reported that it will report fourth quarter and full year 2019 financial results and provide a corporate update on Thursday, March 12, 2020 (Press release, Harpoon Therapeutics, MAR 5, 2020, View Source [SID1234555231]). Harpoon’s management will host a webcast and conference call at 4:30 p.m. ET / 1:30 p.m. PT.

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The live call may be accessed by dialing 866-951-6894 for domestic callers and 409-216-0624 for international callers and entering the conference code: 5468929. A live webcast and archive of the call will be available online from the investor relations section of the company website at www.harpoontx.com.

Bellicum to Report Fourth Quarter and Full Year 2019 Financial Results and Provide Corporate Update

On March 5, 2020 Bellicum Pharmaceuticals, Inc. (NASDAQ:BLCM), a leader in developing novel, controllable cellular immunotherapies for cancers, reported it will report financial results for the fourth quarter and full year 2019 after the close of U.S. markets on Thursday, March 12, 2020 (Press release, Bellicum Pharmaceuticals, MAR 5, 2020, View Source [SID1234555230]). Management will host a webcast and conference call at 5 p.m. ET / 2 p.m. PT that day to discuss the financial results and provide a corporate update.

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The live call may be accessed by dialing 877-407-3103 (U.S. domestic) and 201-493-6791 (international) at least 10 minutes prior to the start of the call. The event will be webcast live and can also be accessed in the Events & Presentations section of bellicum.com. An archived version of the webcast will be available for replay in the Investors & Media section of the Bellicum website following the call.

Actinium Pharmaceuticals Announces First Patient Treated in Third and Final Dose Cohort of Actimab-A CLAG-M Combination Phase 1 Trial in Acute Myeloid Leukemia

On March 5, 2020 Actinium Pharmaceuticals, Inc. (NYSE AMERICAN: ATNM) ("Actinium") reported that the first patient has begun treatment in the third and final cohort of the Actimab-A CLAG-M combination trial (Press release, Actinium Pharmaceuticals, MAR 5, 2020, View Source [SID1234555229]). This Phase 1 trial is an investigator-initiated trial being conducted at the Medical College of Wisconsin in patients with relapsed or refractory acute myeloid leukemia (AML). Patients in the third cohort will receive a cycle of CLAG-M (cladribine, cytarabine, G-CSF, and mitoxantrone) followed by 0.75 uCi/kg of Actimab-A on day 6, 7 or 8. Actimab-A is an antibody radiation conjugate (ARC) that targets the CD33 receptor on blood cancer cells and delivers potent cytotoxic radiation via the radioisotope Actinium-225. This trial will enroll up to 18 patients and will evaluate the safety of this combination including determining the maximum-tolerated dose as well as response rates, progression-free survival and overall survival. Actinium expects the third cohort to be completed mid-2020.

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Patients in the trial to date have been high-risk with intermediate and poor risk cytogenetics with most patients having received three or more prior therapies including bone marrow transplant in some patients. Patients in the first cohort received 0.25 uCi/kg of Actimab-A and the second cohort received 0.50 uCi/kg of Actimab-A. In a prior Phase 1/2 trial of Actimab-A single agent in newly diagnosed AML with 58 patients the 0.5 uCi/kg dose was sub-therapeutic (with response rates of 17%, 22% and 69% at doses of 1.0, 1.5 and 2.0 uCi/kg respectively). In this trial, the second cohort with CLAG-M plus the sub-therapeutic 0.5 uCi/kg dose showed that 86% (6/7) of patients achieved complete remission (CR/CRi) after receiving the 0.50 uCi/kg dose. This is a nearly 60% increase over the remission rate reported in a trial of seventy-four patients with relapsed or refractory AML who received CLAG-M alone. Further, 71% (5/7) of patients achieved negative minimal residual disease (MRD) status following treatment with the combination. MRD negative status means the patient had no detectable disease after treatment. Assuming a successful outcome of the Phase 1 trial, Actinium intends to advance this combination to a Phase 2 randomized trial to demonstrate significance.

"These rates of high complete remission and MRD negative status are not easily achieved in AML let alone in patients with high-risk relapsed or refractory disease. However, AML, and other hematologic cancers, are highly radiation sensitive. Targeting the CD33 receptor on AML cells with potent alpha radiation via an Actinium-225 ARC hits these cells with a cytotoxic agent they have not been exposed to before and have no resistance mechanism against. The result is significant DNA damage that can have a profound anti-tumor effect via targeted delivery that overcomes the limitations of current radiation delivery methods," stated Dr. Mark Berger, Actinium’s Chief Medical Officer. "It is exciting to see data supporting our hypothesis that improved outcomes can be achieved with an ARC therapy in combination with chemotherapy. We feel these results support the additive benefits, mechanistic synergy and potentiating abilities of ARC combinations. We have great excitement for the third and final cohort and hope to improve on the already encouraging results we have seen thus far."

Remission rates achieved with Actimab-A in combination with CLAG-M in this Phase 1 trial compare favorably to targeted agents recently approved for patients with relapsed or refractory AML.

Agent or Regimen

Overall Response Rates

Actimab-A + CLAG-M

86%

Gilteritinib (FLT3 inhibitor)1

68%

Venetoclax + HMA2

64%

Enasidenib (IDH2 inhibitor)3

40%

Venetoclax4

19%

Azacytidine (HMA)5

17%

Actinium intends to explore a larger, randomized Phase 2 and potentially pivotal trial to confirm these preliminary results and provide support for approval of Actimab-A.

Sources:

1. Perl et al. Gilteritinib or Chemotherapy for Relapsed or Refractory FLT3-Mutated AML. N Engl J Med. 2019 Oct 31;381(18):1728-1740.

2. Aldoss et al. Efficacy of the combination of venetoclax and hypomethylating agents in relapsed/refractory acute myeloid leukemia. Haematologica. 2018 Sep;103(9):e404-e407.

3. Stein et al. Enasidenib in mutant IDH2 relapsed or refractory acute myeloid leukemia. Blood. 2017 Aug 10;130(6):722-731.

4. Konopleva et al. Efficacy and Biological Correlates of Response in a Phase II Study of Venetoclax Monotherapy in Patients with Acute Myelogenous Leukemia. Cancer Discov. 2016 Oct;6(10):1106-1117.

5. Itzykson et al. Azacitidine for the treatment of relapsed and refractory AML in older patients. Leuk Res. 2015 Feb;39(2):124-30.