NNW News – Genprex Inc. (GNPX) Making Headway in Clinical Program Expansion, Company Growth

Genprex Inc. (GNPX) Making Headway in Clinical Program Expansion, Company Growth


Related Editorial
Biotech and biopharma industry leaders are posting record financials and hitting milestone markers in their research and growth, good indicators of a strong market with potential for robust returns on investment.

Genprex Inc. (NASDAQ: GNPX) (GNPX Profile) has completed key steps in its overall strategy to expand its clinical development programs and bring Oncoprex(TM) immunogene therapy, its lead drug candidate, to commercialization. Over the past five years, Amgen Inc. (NASDAQ: AMGN) has invested nearly $19 billion in R&D and, as a result, is now advancing a record number of clinical assets. Biogen Inc. (NASDAQ: BIIB) has added four new programs to its pipeline this quarter alone as the company continues to diversify and build depth within neuroscience and pursue therapeutic adjacencies. Celgene Corporation (NASDAQ: CELG) announced recently that its stockholders voted to approve the company’s proposed combination with Bristol-Myers Squibb Company (NYSE: BMY). This key milestone brings the two complementary biopharmaceutical companies one step closer to combining their efforts on a shared mission of discovering, developing and delivering innovative medicines for patients with serious diseases.

To view the full editorial, visit http://nnw.fm/jfD6C

About Genprex, Inc.

Genprex, Inc. is a clinical stage gene therapy company developing potentially life-changing technologies for cancer patients, based upon a unique proprietary technology platform, including Genprex’s initial product candidate, Oncoprex(TM) immunogene therapy for non-small cell lung cancer (NSCLC). Genprex’s platform technologies are designed to administer cancer fighting genes by encapsulating them into nanoscale hollow spheres called nanovesicles, which are then administered intravenously and taken up by tumor cells where they express proteins that are missing or found in low quantities. Oncoprex has a multimodal mechanism of action whereby it interrupts cell signaling pathways that cause replication and proliferation of cancer cells, re-establishes pathways for apoptosis, or programmed cell death, in cancer cells, and modulates the immune response against cancer cells. Oncoprex has also been shown to block mechanisms that create drug resistance. For more information, visit the company’s website at www.Genprex.com.

NOTE TO INVESTORS: The latest news and updates relating to GNPX are available in the company’s newsroom at http://nnw.fm/GNPX

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Pharma Mergers and Acquisitions: Who’s Really Winning Here?

Pharma Mergers and Acquisitions: Who’s Really Winning Here?

(Note: companies that could be impacted by the content of this article are listed at the base of the story (desktop version). This article uses third-party references to provide a bullish, bearish and balanced point of view; sources listed in the “Balanced” section)

The Big Pharma companies in the game including Pfizer Inc., Novartis, and Johnson & Johnson seem to enjoy M&A deals, specifically with small cap biotech stocks. The pharmaceutical giants acquire smaller companies that have patents or technological advancements that they are lacking. Most of these small companies that are acquired do not have sufficient capital to sustain long-term growth. Therefore, mergers and acquisitions deals are important for pharma company growth, but can too many mergers harm the environment in which they operate?

Research – Trovagene (TROV) – Progressing Prostate Cancer Data in Small Number of Patients

Tuesday, August 27, 2019

Trovagene Inc. (TROV)

Progressing Prostate Cancer Data in Small Number of Patients

TrovaGene Inc is a US-based life science company which focuses on the development and commercialization of a proprietary molecular genetic detection technology for use in pharmaceutical development, clinical research and medical testing across a variety of clinical disciplines, including oncology and virology.

Ahu Demir, Ph.D., Biotechnology Research Analyst, Noble Capital Markets, Inc.

Refer to full report for price target, fundamental analysis and rating.

  • Data presentation at APCC.   Trovagene presented data from the Phase 2 Study of
    Onvansertib in combination with Zytiga in patients with metastatic castration-resistant prostate cancer (mCRPC) at the 20th Asia-Pacific Prostate Cancer Conference. The data showed that two out of the four patients who tested positive for androgen receptor splice variant 7 (AR-V7) achieved the primary endpoint of disease control. As presented in ASCO, AR-V7 has been associated with poor prognosis and hormone therapy resistance in mCRPC patients (based on results from a prospective-blinded study (PROPHECY).
  • Still early to speculate clinical benefit.  We believe it is still early to speculate
    Onvansertib’s clinical efficacy in patients with mCRPC. We recognize the strong…



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This Company Sponsored Research is provided by Noble Capital Markets, Inc., a FINRA and S.E.C. registered broker-dealer (B/D).

*Analyst
certification and important disclosures included in full report. 
NOTE: investment decisions should not be based upon the content of
this research summary.  Proper due diligence is required before
making any investment decision.
 

Trovagene Presents Positive Clinical Data from Ongoing Phase 2 Study of Onvansertib in Metastatic Castration-Resistant Prostate Cancer (mCRPC)

Trovagene Presents Positive Clinical Data from Ongoing Phase 2 Study of Onvansertib in Metastatic Castration-Resistant Prostate Cancer (mCRPC)

  • Trial leads to discovery that onvansertib stops rise in PSA in patients with treatment-resistant, highly-aggressive and difficult-to-treat androgen-receptor variant 7 (AR-V7) tumors
  • Data demonstrates efficacy of onvansertib in patients showing early signs of resistance to androgen receptor signaling (ARS) inhibitor, Zytiga®
  • Addition of onvansertib appears to extend the duration of response to ARS inhibitor therapy in this incurable and lethal cancer

SAN DIEGO, Aug. 26, 2019 /PRNewswire/ — 
Trovagene, Inc. (Nasdaq: TROV), a clinical-stage, Precision Cancer Medicine™ oncology therapeutics company developing drugs that target cell division (mitosis), for the treatment of various cancers including prostate, colorectal and leukemia, today announced the presentation of positive clinical data from its ongoing Phase 2 clinical trial of onvansertib in combination with Zytiga® (abiraterone acetate)/prednisone, an androgen-receptor signaling (ARS) inhibitor, in metastatic Castration-Resistant Prostate Cancer (mCRPC), at the 20th Asia-Pacific Prostate Cancer Conference in Melbourne, Australia. These data demonstrate the efficacy of onvansertib in patients showing resistance to the ARS inhibitor, Zytiga® (Johnson & Johnson), including those with the highly-aggressive and difficult-to-treat androgen receptor variant 7 (AR-V7) tumor.

Trovagene is a clinical-stage oncology therapeutics company, using a precision medicine predictive biomarker approach to develop drugs that target cell division (mitosis) for the treatment of leukemias, lymphomas and solid tumor cancers. Onvansertib, its lead drug candidate, is a first-in-class, 3rd generation, highly-selective oral Polo-like Kinase 1 (PLK1) Inhibitor.  The Company currently has two ongoing open-label clinical trials: a Phase 1b/2 trial in acute myeloid leukemia (AML) and a Phase 2 trial in metastatic castration-resistant prostate cancer (mCRPC).

“We have discovered that adding onvansertib to daily ARS inhibitor therapy changes the trajectory of resistance in patients harboring AR-V7, as demonstrated by the immediate decrease in serum PSA levels in patients showing initial signs of resistance to Zytiga®,” said Mark Erlander, PhD, Chief Scientific Officer of Trovagene. “The inhibition of the PLK1 enzyme by onvansertib appears to enhance the efficacy of Zytiga® by repressing the ARS pathway, which is consistent with preclinical data.”

In the ongoing Phase 2 clinical trial of onvansertib, a first-in-class, oral and highly-selective PLK1 inhibitor, patients are being tested with a simple blood test to assess whether they are positive for AR-V7.  In all four patients who tested positive for AR-V7, thus far, an immediate decrease in their serum PSA levels was observed. To-date, two of these patients have achieved the primary efficacy endpoint of disease control. Importantly, while on Zytiga® alone the PSA level for one of the AR-V7 positive patients had a greater than five-fold rise in the two months prior to enrollment and treatment in the trial. Once onvansertib was added to Zytiga®, the patient’s PSA level stopped rising and immediately decreased; the patient remains on treatment.

Additionally, since presenting early data at the American Association for Cancer Research in April, a second arm (Arm B) with a two-week dosing schedule and 50% greater drug exposure to onvansertib over the treatment course, was added to the trial. Preliminary efficacy with PSA stabilization or reduction was observed in the initial three patients enrolled, suggesting that a shorter dosing schedule may maximize response to treatment. Importantly, no unexpected, off-target toxicities have been reported in patients treated to-date.

mCRPC is an incurable and lethal cancer. Nearly all patients with prostate cancer will progress to castration resistance, indicated by increasing serum PSA levels despite castrate levels of testosterone and progress to metastases. 10% to 20% of prostate cancers progress to castration resistant prostate cancer (CRPC) within 5 years of diagnosis, and 84% of newly diagnosed CRPC have metastases. The median survival of patients following diagnosis of castration resistance ranges between 15 and 36 months. The standard-of-care first-line treatment are ARS inhibitors, Zytiga® (Johnson & Johnson) or Xtandi® (Pfizer); however, resistance to these drugs typically develops within 9 to 15 months of initiating treatment. Additionally, up to 30% of patients have the highly-aggressive and ARS-resistant AR-V7. These patients have a shorter progression-free survival (PFS), overall survival (OS) and a poor prognosis. Current treatment for these patients is limited to toxic chemotherapy and there are no effective targeted therapies available.

About Onvansertib

Onvansertib is a first-in-class, third-generation, oral and highly-selective adenosine triphosphate (ATP) competitive inhibitor of the serine/threonine polo-like-kinase 1 (PLK1) enzyme, which is over-expressed in multiple cancers including leukemias, lymphomas and solid tumors. Onvansertib targets the PLK1 isoform only (not PLK2 or PLK3), is orally administered and has a 24-hour half-life with only mild-to-moderate side effects reported. Trovagene believes that targeting only PLK1 and having a favorable safety and tolerability profile, along with an improved dose/scheduling regimen will significantly improve on the outcome observed in previous studies with a former panPLK inhibitor in AML.

Onvansertib has demonstrated synergy in preclinical studies with numerous chemotherapies and targeted therapeutics used to treat leukemias, lymphomas and solid tumor cancers, including irinotecan, FLT3 and HDAC inhibitors, taxanes and cytotoxins. Trovagene believes the combination of onvansertib with other compounds has the potential to improve clinical efficacy in acute myeloid leukemia (AML), metastatic castration-resistant prostate cancer (mCRPC), non-Hodgkin lymphoma (NHL), colorectal cancer and triple-negative breast cancer (TNBC), as well as other types of cancer.

Trovagene has an ongoing Phase 2 clinical trial of onvansertib in combination with Zytiga® (abiraterone acetate)/prednisone in patients with mCRPC who are showing signs of early progressive disease (rise in PSA but minimally symptomatic or asymptomatic) while currently receiving Zytiga®. The trial was accepted by the NLM and is now posted to www.clinicaltrials.gov, with a NCT number of NCT03414034.

Trovagene has an ongoing Phase 1b/2 Study of onvansertib in combination with FOLFIRI and Avastin® for second-line treatment in patients with mCRC with a KRAS mutation. The trial was accepted by the NLM and is now posted to www.clinicaltrials.gov, with a NCT number of NCT03829410. The trial is being conducted at three prestigious cancer centers: USC Norris Comprehensive Cancer Center, Hoag Cancer Center and The Mayo Clinic.

Trovagene has an ongoing Phase 1b/2 clinical trial of onvansertib in combination with low-dose cytarabine or decitabine in patients with relapsed or refractory AML that was accepted by the National Library of Medicine (NLM) and is now posted to www.clinicaltrials.gov, with a NCT number of NCT03303339. Onvansertib has been granted orphan drug designation by the FDA in the U.S. and by the EC in the European Union for the treatment of patients with AML. 

Trovagene licensed onvansertib (also known as NMS-1286937 and PCM-075) from Nerviano Medical Sciences (NMS), the largest oncology-focused research and development company in Italy, and a leader in protein kinase drug development. NMS has an excellent track record of licensing innovative drugs to pharma/biotech companies, including Array (recently acquired by Pfizer), Ignyta (acquired by Roche) and Genentech.

About Trovagene, Inc.

Trovagene is a a clinical-stage, Precision Cancer Medicine™ oncology therapeutics company developing drugs that target cell division (mitosis), for the treatment of various cancers including leukemias, lymphomas and solid tumors. Trovagene has intellectual property and proprietary technology that enables the Company to analyze circulating tumor DNA (ctDNA) and clinically actionable markers to identify patients most likely to respond to specific cancer therapies. Trovagene plans to continue to vertically integrate its tumor genomics technology with the development of targeted cancer therapeutics.  For more information, please visit 
https://www.trovageneoncology.com.

Forward-Looking Statements

Certain statements in this press release are forward-looking within the meaning of the Private Securities Litigation Reform Act of 1995. These statements may be identified by the use of words such as “anticipate,” “believe,” “forecast,” “estimated” and “intend” or other similar terms or expressions that concern Trovagene’s expectations, strategy, plans or intentions. These forward-looking statements are based on Trovagene’s current expectations and actual results could differ materially.  There are a number of factors that could cause actual events to differ materially from those indicated by such forward-looking statements.  These factors include, but are not limited to, our need for additional financing; our ability to continue as a going concern; clinical trials involve a lengthy and expensive process with an uncertain outcome, and results of earlier studies and trials may not be predictive of future trial results; our clinical trials may be suspended or discontinued due to unexpected side effects or other safety risks that could preclude approval of our product candidates; uncertainties of government or third party payer reimbursement; dependence on key personnel; limited experience in marketing and sales; substantial competition; uncertainties of patent protection and litigation; dependence upon third parties; our ability to develop tests, kits and systems and the success of those products; regulatory, financial and business risks related to our international expansion and risks related to failure to obtain FDA clearances or approvals and noncompliance with FDA regulations. There are no guarantees that any of our technology or products will be utilized or prove to be commercially successful.  Additionally, there are no guarantees that future clinical trials will be completed or successful or that any precision medicine therapeutics will receive regulatory approval for any indication or prove to be commercially successful. Investors should read the risk factors set forth in Trovagene’s Form 10-K for the year ended December 31, 2018, and other periodic reports filed with the Securities and Exchange Commission.  While the list of factors presented here is considered representative, no such list should be considered to be a complete statement of all potential risks and uncertainties. Unlisted factors may present significant additional obstacles to the realization of forward-looking statements. Forward-looking statements included herein are made as of the date hereof, and Trovagene does not undertake any obligation to update publicly such statements to reflect subsequent events or circumstances.

Trovagene Contact: 
Vicki Kelemen 
VP, Clinical Development and Investor Relations 
858-952-7652 

[email protected] 

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SOURCE Trovagene, Inc.

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Growing Industry: What Should We Look For?

Growing Industry: What Should We Look For?

(Note: companies that could be impacted by the content of this article are listed at the base of the story (desktop version). This article uses third-party references to provide a bullish, bearish and balanced point of view; sources listed in the “Balanced” section) 

The cannabis industry has been a hot topic in headline news for the past couple of years. Many investors dive into this industry because it’s trending but have no idea where to put their money or what companies are doing to get ahead. It’s important to know the basics of the cannabis industry and to keep up with the laws surrounding the use and distribution, since this affects the growth outlook for cannabis stocks.

Research – Onconova Therapeutics (ONTX) – Inflection Points Ahead

Thursday, August 15, 2019

Onconova Therapeutics (ONTX)

Multiple Value Driving Inflection Points in Near to Medium Term Horizon

Onconova Therapeutics, Inc., a clinical-stage biopharmaceutical company, focused on discovering and developing small molecule inhibitors to treat cancer. The lead product candidate rigosertib is in Phase 3 clinical trial for patients with higher risk myelodysplastic syndromes (MDS). The company has a license agreement with SymBio Pharmaceuticals Limited, development, and commercialization agreement with Pint International; and a license and collaboration agreement with HanX Biopharmaceuticals. Onconova Therapeutics, Inc. was founded in 1998 and is headquartered in Newtown, Pennsylvania.

Ahu Demir, Senior Research Analyst, Noble Capital Markets, Inc.

Refer to full report for price target, fundamental analysis and rating.

  • Onconova’s main focus is INSPIRE.  The company is on track to complete enrollment of Phase 3 study (INSPIRE) with rigosertib, a RAS pathway inhibitor, for the treatment of 2nd line high-risk myelodysplastic syndrome (HR-MDS). Completion of enrolment is expected in H2 2019, data readout to follow in H1 2020.
  • Key Value Driving Catalysts.   Although topline data readout from INSPIRE trial remains as the major milestone for Onconova, we believe achieving the following milestones will generate inflection points for the company; 1) completion of enrollment in INSPIRE study in H2 2019, 2) finalization of…



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This Company Sponsored Research is provided by Noble Capital Markets, Inc., a FINRA and S.E.C. registered broker-dealer (B/D).

*Analyst
certification and important disclosures included in full report. 
NOTE: investment decisions should not be based upon the content of
this research summary.  Proper due diligence is required before
making any investment decision.
 

Research – ProMIS Neurosciences (PMN:CA) – Strengthening Drug Portfolio by Adding Novel Alzheimer’s Antibodies

Wednesday, August 14, 2019

ProMIS Neurosciences (PMN:CA)

Strengthening Drug Portfolio by Adding Novel Alzheimer’s Antibodies

ProMIS Neurosciences, Inc., a development stage biotech company, discovers and develops precision medicine therapeutics for the treatment of neurodegenerative diseases, primarily Alzheimer’s disease (AD) and amyotrophic lateral sclerosis (ALS).

Cosme Ordonez, MD, Ph.D., Senior Life Sciences Analyst, Noble Capital Markets, Inc.

Refer to full report for price target, fundamental analysis and rating.

  • Identification of novel drug candidates for the treatment of Alzheimer’s disease.  Q2/2019, ProMIS Neurosciences identified several antibody drug candidates targeting the protein Tau, which is a primary pharmaceutical target for the treatment of Alzheimer’s disease.
  • Robust drug portfolio. ProMIS has now developed antibodies against toxic oligomers derived from two primary Alzheimer’s targets, Tau and Amyloid beta. In addition, the company’s drug portfolio includes…



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This Company Sponsored Research is provided by Noble Capital Markets, Inc., a FINRA and S.E.C. registered broker-dealer (B/D).

*Analyst
certification and important disclosures included in full report. 
NOTE: investment decisions should not be based upon the content of
this research summary.  Proper due diligence is required before
making any investment decision.
 

Research – electroCore (ECOR) – Soothing Investors’ Migraine a Bit?

Wednesday, August 14, 2019

electroCore (ECOR)

Soothing Investors’ Migraine a Bit?

electrocore Inc is a commercial-stage bioelectronic medicine company with a platform for non-invasive vagus nerve stimulation therapy initially focused on neurology and rheumatology. Its product gammaCore is FDA-cleared for the acute treatment of pain associated with migraine and episodic cluster headache in adults.

Ahu Demir, Biotechnology Research Analyst, Noble Capital Markets, Inc.

Refer to full report for price target, fundamental analysis and rating.

  • Revenue is growing.  The company reported $0.6 million of revenue (+52%), 1,000 paid prescriptions (+52%) and 2,451 prescribing physicians (+11%) in this quarter relative to the previous quarter.
  • Calming of chopping waters. We believe the recent numbers represent a positive trend, following multiple gloomy news in previous quarter. The current revenue ramp-up was driven by…



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This Company Sponsored Research is provided by Noble Capital Markets, Inc., a FINRA and S.E.C. registered broker-dealer (B/D).

*Analyst
certification and important disclosures included in full report. 
NOTE: investment decisions should not be based upon the content of
this research summary.  Proper due diligence is required before
making any investment decision.
 

Research – Dyadic International (DYAI) – Data and Additional Partnerships to Expand Further Value

Wednesday, August 14, 2019

Dyadic (DYAI)

Data and Additional Partnerships to Expand Further Value

Dyadic International, Inc. is a global biotechnology company which is developing what it believes will be a potentially significant biopharmaceutical gene expression platform based on the industrially proven hyper productive engineered fungus Thermothelomyces heterothallica (formerly Myceliophthora thermophila), named C1.
The C1 microorganism, which enables the development and large scale manufacture of low cost proteins, has the potential to be further developed into a safe and efficient expression system that may help speed up the development, lower production costs and improve the performance of biologic vaccines and drugs at flexible commercial scales. Dyadic is using the C1 technology and other technologies to conduct research, development and commercial activities for the development and manufacturing of human and animal vaccines and drugs, such as virus like particles (VLPs) and antigens, monoclonal antibodies, Fab antibody fragments, Fc-Fusion proteins, biosimilars and/or biobetters, and other therapeutic proteins. Dyadic pursues research and development collaborations, licensing arrangements and other commercial opportunities with its partners and collaborators to leverage the value and benefits of these technologies in development and manufacture of biopharmaceuticals. In particular, as the aging population grows in developed and undeveloped countries, Dyadic believes the C1 technology may help bring biologic vaccines, drugs and other biologic products to market faster, in greater volumes, at lower cost, and with new properties to drug developers and manufacturers, and improve access and cost to patients and the healthcare system, but most importantly save lives.

Ahu Demir, Biotechnology Research Analyst, Noble Capital Markets, Inc.

Refer to full report for price target, fundamental analysis and rating.

  • Progressing Towards Validation of Technology.  We continue to believe that the major inflection point for DYAI shares is further validation of C1 technology in biologic manufacturing, data expected by year-end 2019. This will also open doors for additional partnership opportunities.
  • Second Quarter Earning Update. On August 13, the company reported $0.4 million in revenues, $0.7 million in R&D expenses and $1.4 million in G&A expenses. Net loss was $2.2 million, or ($0.08) per share. The reported numbers are in line with…



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This Company Sponsored Research is provided by Noble Capital Markets, Inc., a FINRA and S.E.C. registered broker-dealer (B/D).

*Analyst
certification and important disclosures included in full report. 
NOTE: investment decisions should not be based upon the content of
this research summary.  Proper due diligence is required before
making any investment decision.
 

Research – Trovagene (TROV) – Inflection Points Later this Year

Monday, August 12, 2019

Trovagene Inc. (TROV)

Additional Data Readouts are the Major Inflection Points in H2 2019

TrovaGene Inc is a US-based life science company which focuses on the development and commercialization of a proprietary molecular genetic detection technology for use in pharmaceutical development, clinical research and medical testing across a variety of clinical disciplines, including oncology and virology.

Ahu Demir, Ph.D., Biotechnology Research Analyst, Noble Capital Markets, Inc.

Refer to full report for price target, fundamental analysis and rating.

  • Opportunity in Multiple Indications. Trovagene continues to make progress in its clinical programs including; 1) Phase 1b/2 study in acute myeloid leukemia (AML), 2) Phase 2 study in metastatic castration-resistant prostate cancer (mCRPC) and 3) Phase 1b/2 trial in KRAS-mutated metastatic colorectal cancer (mCRC). 
     
  • Key Value Driving Catalysts. In our view, additional data readouts, validating the potential of Onvansertib in these indications, will unlock additional value for the shares. The nearest-term catalyst is…




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This Company Sponsored Research is provided by Noble Capital Markets, Inc., a FINRA and S.E.C. registered broker-dealer (B/D).

*Analyst
certification and important disclosures included in full report. 
NOTE: investment decisions should not be based upon the content of
this research summary.  Proper due diligence is required before
making any investment decision.
 

Research – TherapeuticsMD (TXMD) – Promising Quarter Signaling to a Positive 2H 2019

Thursday, August 8, 2019

TherapeuticsMD (TXMD)

Promising Quarter Signaling to a Positive 2H 2019

TherapeuticsMD Inc is a major drug manufacturing with a focus on creating and commercializing products targeted exclusively for women. The company intends to commercialize advanced hormone therapy pharmaceutical products.

Ahu Demir, Research Analyst, Noble Capital Markets, Inc.

Refer to full report for price target, fundamental analysis and rating.

  • Exceeded our expectations. TherapeuticsMD reported the second quarter revenues of $6.1million (mm) beating our estimate ($4.7mm). The company also slightly raised full year 2019 revenue guidance to a range of $29.5-34.2mm from $27.1 to 33.1mm. This increase was derived from prenatal vitamin business, rather than FDA approved product revenues.
  • Increasing payers coverage is fundamental. The company is on track securing last few top commercial (covering 71% commercial lives) and Part D payers. The contract amendments and decisions are expected…




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*Analyst
certification and important disclosures included in full report. 
NOTE: investment decisions should not be based upon the content of
this research summary.  Proper due diligence is required before
making any investment decision.
 

Industry Report – Biotechnology Overview

Wednesday, August 7, 2019

Biotechnology YTD

Biotechnology Industry Overview

Ahu Demir, Ph.D., Biotechnology Research Analyst & Cosme Ordonez, M.D., Ph.D, Senior Life Sciences Analyst, Noble Capital Markets, Inc.

Refer to end of report for Analyst Certification & Disclosures

  • Index Performances: NYSE Arca Biotechnology (BTK, +5.8%) and NASDAQ Biotechnology (NBI, +5.6%) have underperformed benchmark indices S&P 500 (SP50, +13.5%) and Russell 3000 (RUA, +13.5%) YTD (as of August 5, 2019) (Exhibit 1). In H1 2019, the stock markets recovered following a steep plunge in Q4 2018. The start of the third quarter has shown a modest slowdown in the markets, including the biotechnology sector.
  • Equity Financing: Overall, biotech financing remained flat in H1 2019 compared to H1 2018. The total monies raised was $4.2 billion. The capital raised by initial public offerings (IPO) in Q1 2019 represented the highest median number since 2011 ($166mm) (Exhibit 5).

  • FDA Approvals: Thus far, U.S. Food and Drug Administration (FDA) has approved 19 drugs in YTD-2019 compared to a record year in 2018 with 59 approvals (Exhibit 12 and 13). 
  • Sector Overview. The biotechnology sector underperformed the broader capital markets in Q2 2019. The lack of major catalysts in the quarter, combined with drug pricing pressure, have had a negative impact on the sector. Going forward, we expect the sector to rebound in the second part of the year, driven by an increase in M&A activity and positive news from ongoing late-stage clinical trials.

Overview

M&A DEALS AS A KEY CATALYST FOR BIOTECHNOLOGY STOCKS

As big pharmaceutical companies continue to face patent expirations, we expect a relatively high level of M&A activity to persist in the biotechnology sector. As such, we expect big pharma to keep hunting for novel promising technologies heating up the M&A barometer in biotech. In our opinion, the primary beneficiary of an M&A wave will be small biotechnology companies, which are built upon innovation. For many years now, small biotechs have attracted the buying power of larger pharmaceutical companies. Going forward, we expect this trend to endure. Although outright acquisitions are one of the main catalysts for the biotech sector, big pharma has also consistently struck high value partnerships with small biotech companies, both private and publicly held. Through strategic collaborations, big pharma gets access to innovative technologies developed by small biotechnology companies, whereas the smaller firms get to see their coffers grow rich by receiving upfront and milestone payments from their larger competitors. All of this is to the delight of biotech investors. 

Bellwether Pfizer is Leading the Charge

In June, big pharma company Pfizer Inc. (PFE) announced its intention to acquire Array BioPharma Inc. (ARRY) for $11.4 billion in cash. Array’s share price skyrocketed 57% on the news. The deal was completed on July 31, 2019. This is the largest acquisition made by Pfizer since the giant pharma company bought Medivation for $14 billion three years ago. The acquisition of Array triggered a rally in the shares of cancer companies as investors hope for similar deals taking place in 2019. By acquiring Array BioPharma, Pfizer added BRAFTOVI (encorafenib) and MEKTOVI (binimetinib) to its product pipeline. These medicines are approved by FDA for the treatment of metastatic melanoma, a type of skin cancer, and are currently being evaluated in Phase III clinical trials for the treatment of metastatic colorectal cancer. Both drugs, encorafenib and binimetinib, target mutations in an oncogene known as BRAF, which is involved in signal transduction pathways controlling cell proliferation. In various human cancers, BRAF gene is mutated leading to tumor growth and progression.

Big Pharma Companies Showing Strong Appetite for Private Biotechnology Companies 

In Q2 2019, Merck & Co.’s management explained to investors that it is looking for small and midsize M&A transactions, especially those expanding its cancer product portfolio to complement Keytruda, the company’s top selling blockbuster drug. Last year, global sales of Keytruda reached $7 billion. In the quarter, Merck bought two privately held companies, Tilos Therapeutics Inc. and Peloton Therapeutics Inc., for $773 million and $1.1 billion, respectively, plus milestone payments. Through the acquisition of Tilos, Merck has now access to candidate medicines targeting the “latent TGF Beta complex” for the treatment of cancer, fibrosis and autoimmune diseases. The transforming growth factor beta (TGF Beta) binds to “latency-associated peptide” (LAP), which is a therapeutic target for various disease indications. TGF Beta plays an instrumental role in inflammation and immune responses. The role of the latency-associated peptide is to regulate TGF Beta functions. Tilos has developed a portfolio of anti-LAP antibodies designed to maximize the therapeutic effects of TGF Beta drugs.

By acquiring Peloton, Merck will add to its oncology drug pipeline a series of novel small molecule therapeutics targeting “HIF-2 alpha” (hypoxia-inducible factor-2 alpha). Peloton’s lead candidate medicine, PT2977, is in late-stage clinical development for the treatment of renal cell carcinoma (RCC). RCC is the most common type of kidney cancer in adults. Under the terms of the agreement, Merck will pay $1.05 billion in cash. Also, Peloton will be eligible to receive $1.15 billion in additional payments upon achieving certain regulatory and commercial milestones. The deal is expected to close in Q3 2019. 

In July, big pharma companies AbbVie (ABBV) and Boehringer Ingelheim announced the acquisitions of Mavupharma and AMAL Therapeutics SA, two privately held biotechnology companies in the cancer area. Mavupharma is focused on the development of novel candidate medicines targeting the STING (“STimulator of INterferon Genes”) pathway for the treatment of cancer. Mavupharma’s lead drug is MAVU-104, a small molecule drug designed to stimulate the STING pathway to induce an anti-cancer immune response. AMAL Therapeutics SA is developing cancer vaccines. AMAL’s lead product is ATP128, a vaccine for the treatment of advanced colorectal cancer, which is expected to enter human clinical trials this quarter. AbbVie and Boehringer did not disclose the financial terms of the deals. 

Gilead Hoping to Stay Competitive by Signing Multiple Strategic Collaborations

Large biotechnology company Gilead (GILD) is building a robust immune-oncology pipeline. In Q2 2019, the bellwether signed two global strategic collaborations with Nurix Therapeutics (private) and Carna Biosciences Inc (CBIXF). Under the terms of the deal with Nurix, Gilead is paying $45 million upfront and up to $2.3 billion in potential milestone payments to add candidate drugs in the “protein degradation area” (targeting the proteasome). Proteasomes are protein complexes located both in the cellular nucleus and cytoplasm, with its main function being getting rid of undesired proteins. The proteasome functions as a “garbage disposal” in the cell. Through the collaboration with Nurix, Gilead will have the option to develop protein degradation drugs for the treatment of cancer and four other diseases.

Under the terms of the deal with Japanese company Carna, Gilead will pay an upfront payment of $20 million. Carna will be eligible to receive up to $450 million in potential milestone payments plus a royalty on future net sales. Gilead will have access to a proprietary platform to develop novel kinase inhibitor drugs targeting cellular lipid signaling. These candidate drugs will be developed for the treatment of cancer.

Outside of cancer, Gilead is also strengthening its leadership position in HIV area. Last month, Gilead signed an agreement with DURECT (DRRX) to get exclusive access to DURECT’s technology (sustained release of long-acting injectable medicines) for the treatment of HIV and HBV (hepatitis B virus) infections. This drug delivery technology enables high drug-loading, controlled onset and sustained release of the medicine for days to months after injection. Gilead paid an upfront payment of $25 million, plus payments of $145 mm upon achieving certain regulatory and sales milestones. In addition, Gilead plans to pay $150 million for any additional products coming out of the collaboration. Since the deal was announced, DURECT’s share price has gained 87%.

Also last month, Gilead signed a 10-year global R&D transformative collaboration with Galapagos NV (GLPG). Gilead will have access to six candidate medicines in human clinical trials, more than 20 preclinical programs and a promising drug discovery platform in exchange for a $3.95 billion upfront payment and $1.1 billion equity investment at a 20% premium to Galapagos’ 30-day, volume-weighted average price. In addition, Galapagos is entitled to milestone payments and royalties. The transaction is expected to close in Q3 2019.

What is in Store for H2 2019

In our view, recent deals are manifestations of a trend, which we expect to persist as a primary catalyst for biotechnology stocks. In Q1 2019, the industry saw M&A deals to surpass the $92 billion mark. Although the deal count is relatively lower in recent months, the relative size of these deals has significantly increased in recent years, with more transactions involving private rather than publicly traded biotech companies (Exhibit 7). Prominent deals in Q1 2019 were the acquisitions of Celgene by Bristol-Myers Squibb for $74 billion, Eli Lilly acquiring Loxo for $8 billion, and Roche acquiring Spark Therapeutics for $4.8 billion. Pharma bellwether Pfizer highlighted Q2 2019 with its $11.4 billion acquisition of Array BioPharma. Investors continue to monitor the industry, eagerly anticipating new M&A developments in the second half of 2019. High value M&A deals and strategic partnerships will be welcome news for biotech investors.

Market Dynamics

Thus far this year, the biotechnology sector has underperformed compared to 2018. With a lower number of FDA drug approvals, amid recent general weakness in the capital markets, biotech investors have stayed on the sidelines. The lack of major catalysts in Q2 2019, combined with drug pricing pressure, have had a negative impact on the sector. In March, Biogen disappointed investors with negative news from its Phase III trials evaluating aducanumab for the treatment of Alzheimer’s disease. The news diminished hopes of finding a potential blockbuster drug for the treatment of Alzheimer’s any time soon. However, we believe that the fundamentals of the biotechnology sector remain healthy, with a number of promising drugs in the pipeline targeting other large commercial opportunities. We expect the sector to rebound in the second part of the year, driven by an increase in M&A activity and positive data from ongoing clinical trials. 

Exhibit 1: Biotechnology Relative Price Performance, YTD 2019 (as of August 5,2019)

Source:  Noble Life Science Research, Capital IQ

S&P 500 (SP50, +13.5%) and Russell 3000 (RUA, +13.5%) benchmark indices have outperformed the NYSE Arca Biotechnology (BTK, +5.8%) and NASDAQ Biotechnology (NBI, +5.6%) indices in YTD- 2019 (as of 8/5/2019). Notable stock price outperformance in the BTK index (in alphabetical order) include Acadia (ACAD, +87.8%), Exact Sciences (EXAS, + 115.1%), Incyte (INCY, +28.4%), Ionis Pharma (IONS, + 42.1%) and Iqvia (IQV, +23.3%).

 

Exhibit 2: Top/Bottom 5 Small Cap Stock Performance, 1 year (as of August 5/2019)

 

Source:  Noble Life Science Research, Capital IQ

Top stock performers of NBI index include Amarin Corporation (AMRN, +529.2%), Ra Pharmaceuticals (RARX, +246.9%), Adverum Biotechnologies (ADVM, + 146.8%), NovoCure Limited (NVCR, +136.0%), Veracyte Inc. (VCYT, +113.9%); bottom performers include Aclaris Therapeutics (ACRS, -94.0%), Zafgen Inc. ( ZFGN, -90.4%), Acorda Therapeutics (ACOR, -88.9%), Lexicon Pharmaceuticals (LXRX,-87.8%) and Unum Therapeutics (UMRX, -87.5%).

 

Exhibit 3: Biotechnology Short Interest % of Float, as of 8/5/19

 

Source: Noble Life Science Research, Capital IQ

Stocks with highest short interest are Opko Health Inc. (OPK), Therapeutics MD (TXMD) and Geron Corporation (GERN).

 

Market Dynamics—Financing

 Exhibit 4: Biotech Financing YTD-2019 (between $50-$200mm)

Source:  Noble Life Science Research, Capital IQ

The largest transactions include Alector Inc. (ALEC, $176mm), Zai Lab Ltd (ZLAB, $200 mm) and Intercept Pharmaceuticals (ICTP, $200 mm).

Exhibit 5: Biotech Financings—IPO and Follow-on Capital Raised by Quarter (Median)

Source:  Noble Life Science Research, Capital IQ

Biotech financings in YTD-2019 has already exceeded the full year of 2018 numbers ($535mm vs. $527mm, respectively). This was a result of large transactions, initial public offering (IPO) in Q1 2019, including Alector Inc. (ALEC, $175mm), Turning Point Pharmaceuticals Inc. (TPTX, $166mm) and Precision Biosciences (DTIL, $126mm).

Exhibit 6: Biotech Licensing Deals

Source:  Noble Life Science Research, Bloomberg

The licensing deal transactions in H1 2019 showed a modest decrease of 5% compared to H1 2018.

Exhibit 7: Biotech M&A Deals

Source:  Noble Life Science Research, Bloomberg

The size of private M&A deals showed an uptick (+19%) in 1H 2019 compared to 1H 2018.

Lock-Up Expirations

Exhibit 8: IPO and Follow-On Lock-Up Expiration Data for 2019 

Source:  Noble Life Science Research, Bloomberg


Selected Industry Conferences

Exhibit 9: Medical, Scientific and Industry Conferences for 2019

Source:  Noble Life Science Research, Biomed Tracker


FDA Approvals

Exhibit 10: Selected Pending Approvals of New Molecule Entities (NMEs) and Biologics

Source: Biomed Tracker, FDA

Exhibit 11: Upcoming Advisory Committee Meeting Dates

Source: Noble Life Science Research, FDA


Exhibit 12: Selected Recently Approved Drugs and Biologics, YTD

Source: Noble Life Science Research, Biomed Tracker, FDA

In total, 19 medicines were approved in YTD-2019. The table does not include the approval of Zolgensma, which instead of a drug is a gene therapy. Zolgensma was developed by AveXis Inc., which was acquired by Novartis in 2018. Zolgensma is the first gene therapy approved for the treatment of spinal muscular atrophy (SMA), a leading cause of death in children. SMA is a rare genetic disease caused by a mutation in the “survival motor neuron 1” (SMN1) gene. Children with SMA cannot perform essential functions of life, cannot hold their heads up, nor can swallow and breath properly.

Drug Landscape

Exhibit 13: New FDA Drug Approvals

Source: Noble Life Science Research, Bloomberg

19 drug approvals in 2019 (YTD) demonstrated a low productive year following all-time record of 59 approvals in 2018.

 

Exhibit 14: Number of Drugs in the Pipeline

Source: Noble Life Science Research, Global Data Intelligence

Oncology continues to be the dominant development category, which we think has also been fueled of late by the 1000+ immuno-oncology clinical drug trials.

Appendix

Exhibit 15: Cash Analysis, sorted by E/P

 

Note: Market cap as of 8/5/2019, Cash value for 2Q19

Source: Noble Life Science Research, Capital IQ


Exhibit 16: Catalyst Calendar (Market Cap $10-250mm)

  

Source: Noble Life Science Research, Biomed Tracker 

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ANALYST CREDENTIALS, PROFESSIONAL DESIGNATIONS, AND EXPERIENCE

Equity Research Analyst focusing on the Life Sciences sector. 5 years of industry experience. PhD in Chemistry from University of Florida.Post-Doctoral training at Columbia University and New York University. Her scientific training focused on antiviral therapy, oncology and immuno-oncology. 
FINRA licenses 7, 63, 86, 87.

Senior Equity Analyst focusing on Life Sciences. More than 16 years of experience in his field. Former President and co-founder of Ciclofilin Pharmaceuticals. Held various roles in Buy-side and Sell-Side specializing in drug development, medical device, specialty pharma and healthcare services areas. Medical Doctor with a Ph.D. in Experimental Medicine and Biochemistry from McGill University in Montreal, Canada. Completed post-doctoral training at the Karolinska Institute/Hospital in Stockholm, Sweden. 
Holds FINRA licenses 7, 79, 86, 87.

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Report ID: 11022