INmune Bio Inc. Announces Second Quarter 2024 Results and Provides Business Update

Rhea-AI Summary

INmune Bio Inc. (NASDAQ: INMB) announced Q2 2024 results and provided a business update. Key highlights include:

1. The Phase 2 trial for XPro™ in Early Alzheimer's Disease is on track to complete enrollment by Q3 end.
2. A new Phase 1b analysis shows XPro's™ significant effects on synaptic proteins.
3. INKmune™ platform progress includes a new formulation and completion of the first cohort in the Phase I/II trial for metastatic castration-resistant prostate cancer.
4. The company raised $14.5 million in equity capital.
5. Q2 2024 financial results: Net loss of $9.7 million, R&D expenses of $7.1 million, and cash position of $31.1 million as of June 30, 2024.

Positive

• Phase 2 trial for XPro™ in Early Alzheimer's Disease on track to complete enrollment by Q3 end
• New Phase 1b analysis shows XPro's™ significant effects on synaptic proteins
• Successful completion of extended stability validation for XPro™
• Completion of first cohort in Phase I/II trial of INKmune™ for mCRPC
• Raised $14.5 million in equity capital
• Received $2.5 million USD in R&D rebates from Australia
• Joined Russell 3000® Index

Negative

• Net loss increased to $9.7 million in Q2 2024 from $6.5 million in Q2 2023
• R&D expenses increased to $7.1 million in Q2 2024 from $4.1 million in Q2 2023
• G&A expenses increased to $2.8 million in Q2 2024 from $2.3 million in Q2 2023

Financial Analyst

INmune Bio's Q2 2024 results reveal a significant increase in net loss to $9.7 million, up from $6.5 million in Q2 2023. This 49% jump in losses is primarily driven by escalated R&D expenses, which rose to $7.1 million from $4.1 million year-over-year. The surge in R&D costs signals an intensification of the company's clinical programs, particularly for XPro™ and INKmune™.

Despite the widening losses, INmune's cash position remains robust at $31.1 million as of June 30, 2024. This financial cushion was bolstered by a $14.5 million equity raise in April and a $2.5 million R&D rebate from Australia in July. The company's inclusion in the Russell 3000® Index could potentially enhance its visibility to institutional investors.

However, investors should note the accelerated cash burn rate. If R&D expenses continue to climb at this pace, INmune may need to seek additional funding within the next 12-18 months, which could lead to dilution. The company's ability to deliver positive clinical results, particularly from its Alzheimer's and prostate cancer trials, will be important in maintaining investor confidence and potentially securing partnerships or non-dilutive funding.

Medical Research Analyst

INmune Bio's pipeline progress, particularly with XPro™ for Alzheimer's Disease (AD), shows promise. The completion of a blinded interim analysis for the Phase II AD trial, confirming appropriate power for primary and secondary endpoints, is a positive signal. Moreover, the new proteomic data presented at AAIC, demonstrating XPro's™ significant effects on synaptic proteins, provides a mechanistic rationale for its potential efficacy.

The extended stability validation for XPro™ (24-month stability at 2C-8C) is a important development, as it addresses a key logistical challenge in drug development and positions the company well for potential Phase III trials and commercialization.

For INKmune™, the completion of the first cohort in the Phase I/II trial for metastatic castration-resistant prostate cancer (mCRPC) and the approval to proceed with the second dose level are important milestones. The safety profile and outpatient administration of INKmune™ are encouraging factors that could facilitate patient recruitment and potentially reduce treatment costs.

However, it's important to note that while these developments are promising, they are still early-stage. The true test will be the top-line data from the Phase II AD trial and the full results from the mCRPC trial. Investors should remain cautious until more definitive efficacy data is available.

Company to Host Conference Call Today, August 1, at 4:30pm ET

BOCA RATON, Fla., Aug. 01, 2024 (GLOBE NEWSWIRE) -- INmune Bio Inc. (NASDAQ: INMB) (the “Company”), a clinical-stage inflammation and immunology company developing treatments that harness the patient’s innate immune system to fight disease, today announces its financial results for the quarter ended June 30, 2024 and provides a business update.

Q2 2024 and Recent Corporate Highlights

DN-TNF Platform Highlights (XPro™):

• The Phase 2 randomized, blinded clinical trial for patients with Early Alzheimer's Disease is on schedule to reach its final enrollment before the end of Q3 followed by top-line data approximately six months from the last patient enrolled.
• Announced completion of blinded interim analysis of the ongoing Phase II Alzheimer’s Disease trial, confirming that the trial is appropriately powered to assess its primary and secondary cognitive endpoints, the Early Mild Alzheimer’s Cognitive Composite (EMACC) and CDR. The third-party evaluation concluded that the trial design, operational execution, data collection, and management are of the highest quality.
• New Phase 1b analysis of proteomic data presented at AAIC shows XPro's™ significant effects on a broad range of synaptic proteins and pathways. The analysis revealed that a 12-week treatment with XPro™ resulted in a significant change in synaptic proteins, which are essential for communication between neurons. The formation and elimination of synapses is executed by cells of the innate immune system such as astrocytes. When these cells are in a dysregulated inflammatory/immune state, synapse formation is reduced and synapse elimination is increased, resulting in loss of communication between neurons which, in the case of AD, results in cognitive impairment. Restoring synapses requires a normally functioning innate immune system.
• The Company successfully completed extended stability validation for XPro™ at continuous storage in solution at 2C-8C. The 24 and 30-month stability test samples passed all chemistry and potency assays allowing the Company to make a conservative claim of 24-month stability and positioning it to meet the dosing demands envisioned in the Phase III trial.
• Shared the progress of two early patients in the Phase 1b AD trial in Australia who have continued to receive XPro™ treatment under an open-label program administered by their treating physician. The video testimonials underscore XPro’s™ unique attributes that may halt progression of cognitive impairment versus existing treatments that slow the pace of, but do not stop the progression of, cognitive decline.

INKmune™ Platform:

• Announced a new formulation of INKmune™ that supports single bag administration at the highest trial dose, and expansion of bioreactor capacity in preparation of scalable manufacturing. An IND amendment with the improved formulation has been submitted to the FDA that also includes additional validation data supporting an alternative critical reagent used in INKmune™ manufacturing, improving supply chain redundancy.
• Completed the first cohort in the Phase I/II open label trial (the “CarePC” trial) of INKmune™ in metastatic castration-resistant prostate cancer (mCRPC). Following review by the Safety Review Committee (SRC), approval was granted to proceed with the second dose level (cohort 2) and two patients have been enrolled. Data from this open-label trial is expected to be released intermittently as it becomes available.
• Patient enrollment in CarePC remains robust and on schedule. The first patient of the middle dose cohort will complete treatment this month and the 2nd patient of the middle dose cohort is about to be screened. The safety of INKmune™ remains excellent and all patients in the CarePC trial have been treated as an out-patient. Data from the trial is expected to be released later this year.
• The most recent pre-clinical data and early clinical results with INKmune™ have been published in the peer-reviewed Journal for ImmunoTherapy of Cancer this month. The study demonstrates that memory-like natural killer (mlNK) cells, generated by either cytokine or INKmune™ priming, show increased cytotoxicity against multiple tumor types, offering promising potential for cancer immunotherapy. Importantly, while most studies are conducted on NK cells from healthy volunteers, this study demonstrated that mlNK from cancer patients are equally as potent as those generated from healthy volunteers, further supporting INKmune™’s in vivo treatment methodology. The research also provides new insights into the metabolic and physiological mechanisms underlying NK cell memory, paving the way for innovative treatments in both hematological malignancies and solid tumors.

Corporate:

• The Company is presenting at BTIG’s Virtual Biotechnology Conference 2024 on Tuesday, August 6, 2024 at 8AM ET and will host one-on-one meetings August 5/6. This conference is being hosted by BTIG, a global financial services firm specializing in institutional trading, investment banking, research and related brokerage services. To join the conference, email uscorporateaccess@btig.com.
• Joined the broad-market Russell 3000® Index at the conclusion of the 2024 Russell US Indexes annual reconstitution, effective as of Monday, July 1^st, 2024.
• The Company successfully raised a combined $14.5 million of equity capital before placement agent fees and expenses in two separate transactions in late April. Of note, in the first $4.8 million offering, management and members of the Board of Directors purchased approximately 20% of the offering. Excluding shares and warrants acquired by insiders, both offerings were priced at-the-market.
• Received a research and development rebates from Australia in July of approximately $2.5 million USD.
  

Upcoming Events and Milestones:

• Full enrollment in the Phase II XPro™ trial for treatment of neuroinflammation as a cause of Alzheimer’s Disease is expected before the end of Q3 followed by top-line data approximately six months from the last patient enrolled.
• Initiate a Phase II trial of XPro™ in patients with Treatment-Resistant Depression 2H 2024.
• Expect to complete enrollment in the Phase I portion of INKmune™ in metastatic castration-resistant prostate cancer trial in Q4 2024. The Phase II portion is expected to complete enrollment in Q2, 2025, however we expect to provide periodic updates on the immunologic and therapeutic response to INKmune as data becomes available.
  

Financial Results for the First Quarter Ended June 30, 2024:

• Net loss attributable to common stockholders for the quarter ended June 30, 2024 was approximately $9.7 million, compared to approximately $6.5 million during the quarter ended June 30, 2023.
• Research and development expenses totaled approximately $7.1 million for the quarter ended June 30, 2024, compared to approximately $4.1 million during the quarter ended June 30, 2023.
• General and administrative expenses were approximately $2.8 million for the quarter ended June 30, 2024, compared to approximately $2.3 million during the quarter ended June 30, 2023.
• Other income (expense), net was approximately $0.1 million for the quarter ended June 30, 2024, compared to approximately ($0.1) million during the quarter ended June 30, 2023.
• As of June 30, 2024, the Company had cash and cash equivalents of approximately $31.1 million.
• As of August 1, 2024, the Company had approximately 19.8 million common shares outstanding.

Earnings Call Information

To participate in this event, dial approximately 5 to 10 minutes before the beginning of the call. Please ask for the INmune Bio Second Quarter Conference Call when reaching an operator.

Date: August 1, 2024
Time: 4:30 PM Eastern Time
Participant Dial-in: 1-800-225-9448
Participant Dial-in (international): 1-203-518-9708
Conference ID: INMUNE

A live audio webcast of the call can be accessed by clicking here or using this link:
https://viavid.webcasts.com/starthere.jsp?ei=1679432&tp_key=8a15b560a4

A transcript will follow approximately 24 hours from the scheduled call. A replay will also be available through August 8, 2024, by dialing 1-844-512-2921 or 1-412-317-6671 (international) and entering PIN no. 11156467.

About XPro™

XPro™ is a next-generation inhibitor of tumor necrosis factor (TNF) that is currently in clinical trial and acts differently than currently available TNF inhibitors in that it neutralizes soluble TNF (sTNF), without affecting trans-membrane TNF (tmTNF) or TNF receptors. XPro™ could have potential substantial beneficial effects in patients with neurologic disease by decreasing neuroinflammation. For more information about the importance of targeting neuroinflammation in the brain to improve cognitive function and restore neuronal communication visit this section of the INmune Bio’s website.

About INKmune™

INKmune™ is a pharmaceutical-grade, replication-incompetent human tumor cell line which conjugates to resting NK cells and delivers multiple, essential priming signals to convert the cancer patient’s resting NK cells into tumor killing memory-like NK cells (mlNK cells). INKmune™ treatment converts the patient’s own NK cells into mlNK cells. In patients, INKmune™ primed tumor killing NK cells have persisted for more than 100 days. These cells function in the hypoxic TME because due to upregulated nutrient receptors and mitochondrial survival proteins.

INKmune™ is a patient friendly drug treatment that does not require pre-medication, conditioning or additional cytokine therapy to be given to the patients. INKmune™ is easily transported, stored and delivered to the patient by a simple intravenous infusion as an out-patient. INKmune™ is tumor agnostic; it can be used to treat many types of NK-resistant tumors including leukemia, lymphoma, myeloma, lung, ovarian, breast, renal and nasopharyngeal cancer. INKmune™ is treating patients in an open label Phase I/II trial in metastatic castration-resistant prostate cancer in the US this year.

About INmune Bio Inc.

INmune Bio Inc. is a publicly traded (NASDAQ: INMB), clinical-stage inflammation and immunology biotechnology company focused on developing treatments that target the innate immune system to fight disease. INmune Bio has two product platforms that are both in clinical trials: The Dominant-Negative Tumor Necrosis Factor (DN-TNF) product platform utilizes dominant-negative technology to selectively neutralize soluble TNF, a key driver of innate immune dysfunction and a mechanistic driver of many diseases. DN-TNF product candidates are in clinical trials to determine if they can treat cancer (INB03™), Early Alzheimer’s disease and treatment-resistant depression (XPro™). The Natural Killer Cell Priming Platform includes INKmune™ developed to prime a patient’s NK cells to eliminate minimal residual disease in patients with cancer. INmune Bio’s product platforms utilize a precision medicine approach for the treatment of a wide variety of hematologic and solid tumor malignancies, and chronic inflammation. To learn more, please visit www.inmunebio.com.

Forward Looking Statements

Clinical trials are in early stages and there is no assurance that any specific outcome will be achieved. Any statements contained in this press release that do not describe historical facts may constitute forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995. Any statements contained in this press release that do not describe historical facts may constitute forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995. Any forward-looking statements contained herein are based on current expectations but are subject to a number of risks and uncertainties. Actual results and the timing of certain events and circumstances may differ materially from those described by the forward-looking statements as a result of these risks and uncertainties. INB03™, XPro1595 (XPro™), and INKmune™ are still in clinical trials or preparing to start clinical trials and have not been approved by the US Food and Drug Administration (FDA) or any regulatory body and there cannot be any assurance that they will be approved by the FDA or any regulatory body or that any specific results will be achieved. The factors that could cause actual future results to differ materially from current expectations include, but are not limited to, risks and uncertainties relating to the Company’s ability to produce more drug for clinical trials; the availability of substantial additional funding for the Company to continue its operations and to conduct research and development, clinical studies and future product commercialization; and, the Company’s business, research, product development, regulatory approval, marketing and distribution plans and strategies. These and other factors are identified and described in more detail in the Company’s filings with the Securities and Exchange Commission, including the Company’s Annual Report on Form 10-K, the Company’s Quarterly Reports on Form 10-Q and the Company’s Current Reports on Form 8-K. The Company assumes no obligation to update any forward-looking statements in order to reflect any event or circumstance that may arise after the date of this release.

INmune Bio Contact:
David Moss
Chief Financial Officer
(858) 964-3720

Daniel Carlson
Head of Investor Relations
(415) 509-4590
dcarlson@inmunebio.com

Investor Contact:
Mike Moyer
Managing Director – LifeSci Advisors
mmoyer@lifesciadvisors.com

The following tables summarize our results of operations for the periods indicated:

INMUNE BIO INC.
CONDENSED CONSOLIDATED BALANCE SHEETS (In thousands, except share and per share amounts) (Unaudited)
		June 30, 2024				December 31, 2023
ASSETS
CURRENT ASSETS
Cash and cash equivalents		$	31,069			$	35,848
Research and development tax credit receivable			3,143				1,905
Other tax receivable			270				537
Prepaid expenses and other current assets			1,013				1,510
Prepaid expenses – related party			-				142
TOTAL CURRENT ASSETS			35,495				39,942
Operating lease – right of use asset			363				414
Other assets			81				131
Acquired in-process research and development intangible assets			16,514				16,514
TOTAL ASSETS		$	52,453			$	57,001
LIABILITIES, REDEEMABLE COMMON STOCK AND STOCKHOLDERS’ EQUITY
CURRENT LIABILITIES
Accounts payable and accrued liabilities		$	9,282			$	7,901
Accounts payable and accrued liabilities – related parties			139				35
Deferred liabilities			521				489
Current portion of long-term debt			4,979				9,921
Operating lease, current liability			130				119
TOTAL CURRENT LIABILITIES			15,051				18,465
Long-term operating lease liability			322				397
TOTAL LIABILITIES			15,373				18,862
COMMITMENTS AND CONTINGENCIES
Redeemable common stock, $0.001 par value; 75,697 shares issued and outstanding (Note 9)			799				799
STOCKHOLDERS’ EQUITY
Preferred stock, $0.001 par value, 10,000,000 shares authorized, 0 shares issued and outstanding			-				-
Common stock, $0.001 par value, 200,000,000 shares authorized, and 19,706,732 and 17,950,776 shares issued and outstanding, respectively			20				18
Additional paid-in capital			178,767				159,143
Accumulated other comprehensive loss			(713	)			(799	)
Accumulated deficit			(141,793	)			(121,022	)
TOTAL STOCKHOLDERS’ EQUITY			36,281				37,340
TOTAL LIABILITIES, REDEEMABLE COMMON STOCK AND STOCKHOLDERS’ EQUITY		$	52,453			$	57,001

INMUNE BIO INC.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS (In thousands, except share and per share amounts) (Unaudited)
		For the Three Months Ended June 30,								For the Six Months Ended June 30,
		2024				2023				2024				2023
REVENUE		$	-			$	46			$	14			$	84
OPERATING EXPENSES
General and administrative			2,812				2,309				5,150				4,637
Research and development			7,053				4,148				15,746				8,281
Total operating expenses			9,865				6,457				20,896				12,918
LOSS FROM OPERATIONS			(9,865	)			(6,411	)			(20,882	)			(12,834	)
OTHER INCOME (EXPENSE), NET			119				(90	)			111				(203	)
NET LOSS		$	(9,746	)		$	(6,501	)		$	(20,771	)		$	(13,037	)
Net loss per common share – basic and diluted		$	(0.50	)		$	(0.36	)		$	(1.11	)		$	(0.73	)
Weighted average common shares outstanding – basic and diluted			19,307,323				17,945,995				18,666,898				17,945,995
COMPREHENSIVE LOSS
Net loss		$	(9,746	)		$	(6,501	)		$	(20,771	)		$	(13,037	)
Other comprehensive income (loss) – foreign currency translation			(44	)			(4	)			86				(13	)
Total comprehensive loss		$	(9,790	)		$	(6,505	)		$	(20,685	)		$	(13,050	)

INMUNE BIO INC.
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS  (In thousands) (Unaudited)
		For the Six Months Ended June 30,
		2024				2023
CASH FLOWS FROM OPERATING ACTIVITIES:
Net loss		$	(20,771	)		$	(13,037	)
Adjustments to reconcile net loss to net cash used in operating activities:
Stock-based compensation			4,129				3,600
Accretion of debt discount			58				125
Changes in operating assets and liabilities:
Research and development tax credit receivable			(1,238	)			6,165
Other tax receivable			267				250
Prepaid expenses			497				1,320
Prepaid expenses – related party			142				4
Other assets			50				(31	)
Accounts payable and accrued liabilities			1,381				(2,821	)
Accounts payable and accrued liabilities – related parties			104				-
Deferred liabilities			32				(56	)
Accrued liability – long-term			-				176
Operating lease liabilities			(13	)			(10	)
Net cash used in operating activities			(15,362	)			(4,315	)
CASH FLOWS FROM FINANCING ACTIVITIES:
Net proceeds from sale of common stock and warrants			15,497				-
Repayments of debt			(5,000	)			-
Net cash provided by financing activities			10,497				-
Impact on cash from foreign currency translation			86				(13	)
NET DECREASE IN CASH AND CASH EQUIVALENTS			(4,779	)			(4,328	)
CASH AND CASH EQUIVALENTS AT BEGINNING OF PERIOD			35,848				52,153
CASH AND CASH EQUIVALENTS AT END OF PERIOD		$	31,069			$	47,825
SUPPLEMENTAL DISCLOSURE OF CASH FLOWS INFORMATION:
Cash paid for income taxes		$	-			$	-
Cash paid for interest expense		$	523			$	930

FAQ

What were INmune Bio's (INMB) Q2 2024 financial results?

INmune Bio reported a net loss of $9.7 million, R&D expenses of $7.1 million, and G&A expenses of $2.8 million for Q2 2024. The company had $31.1 million in cash and cash equivalents as of June 30, 2024.

What is the status of INmune Bio's (INMB) XPro™ Phase 2 trial for Alzheimer's Disease?

The Phase 2 randomized, blinded clinical trial for XPro™ in Early Alzheimer's Disease is on schedule to complete enrollment by the end of Q3 2024, with top-line data expected approximately six months after the last patient is enrolled.

What progress has INmune Bio (INMB) made with its INKmune™ platform?

INmune Bio announced a new formulation of INKmune™ supporting single bag administration, completed the first cohort in the Phase I/II trial for metastatic castration-resistant prostate cancer, and received approval to proceed with the second dose level.

How much capital did INmune Bio (INMB) raise in Q2 2024?

INmune Bio successfully raised a combined $14.5 million of equity capital before placement agent fees and expenses in two separate transactions in late April 2024.